Adaptors for removing medicinal fluids from a container

ABSTRACT

In certain embodiments, a vial adaptor for removing liquid contents from a vial includes a piercing member and a bag. The bag can be contained within the piercing member such that the bag is introduced to the vial when the vial adaptor is coupled with the vial. In some embodiments, the bag expands within the vial as liquid is removed from the vial via the adaptor, thereby regulating pressure within the vial. In other embodiments, a vial includes a bag for regulating pressure within the vial as liquid is removed therefrom. In some embodiments, a vial adaptor is coupled with the vial in order to remove the liquid. In some embodiments, as the liquid is removed from the vial via the adaptor, the bag expands within the vial, and in other embodiments, the bag contracts within the vial.

INCORPORATION BY REFERENCE TO ANY PRIORITY APPLICATIONS

Any and all applications for which a foreign or domestic priority claimis identified in the Application Data Sheet as filed with the presentapplication are incorporated by reference under 37 CFR 1.57 and made apart of this specification.

BACKGROUND

1. Field

Certain embodiments disclosed herein relate to novel adaptors forcoupling with medicinal vials, and novel medicinal vials, to aid in theremoval of contents from the vials and/or to aid in the injection ofsubstances therein, while regulating pressure within such vials.

2. Description of Related Art

It is a common practice to store medicines or other medically relatedfluids in vials. In some instances, the medicines or fluids so storedare therapeutic if injected to the bloodstream, but harmful if inhaledor if contacted by exposed skin. Certain known systems for extractingpotentially harmful medicines from vials suffer from various drawbacks.

SUMMARY

In certain embodiments, a vial adaptor for removing liquid contents froma vial comprises a piercing member and a bag. The bag can be containedwithin the piercing member such that the bag is introduced to the vialwhen the vial adaptor is coupled with the vial. In some embodiments, thebag expands within the vial as liquid is removed from the vial via theadaptor, thereby regulating pressure within the vial.

In other embodiments, a vial comprises a bag for regulating pressurewithin the vial as liquid is removed therefrom. In some embodiments, avial adaptor is coupled with the vial in order to remove the liquid. Insome embodiments, as the liquid is removed from the vial via theadaptor, the bag expands within the vial, and in other embodiments, thebag contracts within the vial.

In further embodiments, a pressure regulating device comprises aconnector configured to couple the device with a vial. The deviceincludes a piercing member having a sheath extending from a base of thepiercing member. The piercing member is configured to be inserted intothe vial when then device is coupled with the vial. An extractoraperture is formed in the sheath and positioned within a region coveringat least about one-eighth of the distance from the base of the piercingmember to an end of the sheath. A bag is adapted to be expanded orunfolded inside the vial. The bag is configured to move from a firstorientation substantially unexpanded or folded to a second orientationat least partially expanded or unfolded and at least partially insidethe vial. The bag is sized and positioned to at least partially fitwithin the vial when the bag is in the second orientation. The bagcomprises a layer that is substantially impermeable to a medicinal fluiddisposed within the vial, thereby impeding the passage of said medicinalfluid between an outer surface and an inner surface of the bag. Thedevice regulates the pressure in the vial such that, as the medicinalfluid is withdrawn from the vial, the bag will expand or unfold in orderto substantially equilibrate pressure on opposite sides of the bag.

BRIEF DESCRIPTION OF THE DRAWINGS

Various embodiments are depicted in the accompanying drawings forillustrative purposes, and should in no way be interpreted as limitingthe scope of the inventions. In addition, various features of differentdisclosed embodiments can be combined to form additional embodiments.

FIG. 1 is a schematic illustration of a system for removing fluid fromand/or injecting fluid into a vial.

FIG. 2 is a schematic illustration of another system for removing fluidfrom and/or injecting fluid into a vial.

FIG. 3 is an illustration of another system for removing fluid fromand/or injecting fluid into a vial.

FIG. 4 is a perspective view of a vial adaptor and a vial.

FIG. 5 is a partial cross-sectional view of the vial adaptor of FIG. 4coupled with a vial in an initial stage.

FIG. 6A is a cross-sectional view depicting a distal portion of apiercing member of a vial adaptor.

FIG. 6B is a cross-sectional view depicting a distal portion of apiercing member of a vial adaptor.

FIG. 7 is a partial cross-sectional view of the vial adaptor of FIG. 4coupled with a vial in a subsequent stage.

FIG. 8 is a partial cross-sectional view of a vial adaptor coupled witha vial.

FIG. 9 is a partial cross-sectional view of a vial adaptor coupled witha vial.

FIG. 10 is a cutaway perspective view of a vial adaptor.

FIG. 11 is a partial cross-sectional view of a vial adaptor coupled witha vial.

FIG. 12A is a cutaway perspective view of a vial adaptor.

FIG. 12B is a partial cutaway perspective view of the vial adaptor ofFIG. 12A coupled with a vial.

FIG. 12C is a cutaway perspective view of a vial adaptor.

FIG. 12D is a partial cutaway perspective view of the vial adaptor ofFIG. 12C coupled with a vial.

FIG. 13 is a partial cross-sectional view of a vial adaptor coupled witha vial.

FIG. 14 is a bottom plan view of a sleeve comprising multiple sleevemembers.

FIG. 15A is a cross-sectional view of a nozzle coupled with a bag.

FIG. 15B is a partial cross-sectional view of a nozzle coupled with abag.

FIG. 16 is a top plan view of a folded bag.

FIG. 17 is a partial cross-sectional view of a vial adaptor coupled witha vial.

FIG. 18 is a partial cross-sectional view of a vial adaptor coupled witha vial.

FIG. 19 is a cross-sectional view of a vial adaptor.

FIG. 20A is a partial front plan view of a tab locking mechanism for avial adaptor.

FIG. 20B is a partial front plan view of a tab locking mechanism for avial adaptor.

FIG. 21 is an exploded perspective view of a vial adaptor.

FIG. 22 is a perspective view of a housing member of the vial adaptor ofFIG. 21.

FIG. 23 is a cross-sectional view of the vial adaptor of FIG. 21 afterassembly.

FIG. 24 is a partial cross-sectional view of a vial adaptor coupled witha vial.

FIG. 25 is a partial cross-sectional view of a vial adaptor coupled witha vial.

FIG. 26 is a top plan view of a cap of a vial.

FIG. 27 is a cross-sectional view of a vial adaptor coupled with a vial.

FIG. 28 is a partial cross-sectional view of a vial.

FIG. 29 is a partial cross-sectional view of a vial adaptor coupled witha vial.

FIG. 30 is an exploded perspective view of a vial adaptor.

FIG. 31 is a side plan view of a housing member of the vial adaptor ofFIG. 30.

FIG. 32 is a partial cross-sectional view of the housing member of FIG.31.

FIG. 33 is a cross-sectional view of the housing member of FIG. 31.

FIG. 34 is another cross-sectional view of the housing member of FIG.31.

FIG. 35 is a perspective view of a plug of the vial adaptor of FIG. 30.

FIG. 36 is a cross-sectional view of the plug of FIG. 35.

FIG. 37 is a bottom plan view of a cap connector of the vial adaptor ofFIG. 30.

FIG. 38 is a cross-sectional view of the cap connector of FIG. 37.

FIG. 39 is a top plan view of the cap connector of FIG. 37.

FIG. 40 is an exploded perspective view of an embodiment of a vialadaptor.

FIG. 41A is a top plan view of an embodiment of a housing membercompatible with certain embodiments of the vial adaptor of FIG. 40.

FIG. 41B is an elevation view of the housing member of FIG. 41A.

FIG. 42 is an elevation view of an embodiment of a bag compatible withcertain embodiments of the vial adaptor of FIG. 40.

FIG. 43A is a cross-sectional view of an embodiment of a bag retainercompatible with certain embodiments of the vial adaptor of FIG. 40.

FIG. 43B is a cross-sectional view of another embodiment of a bagretainer compatible with certain embodiments of the vial adaptor of FIG.40.

FIG. 44A is an elevation view of the vial adaptor of FIG. 40 in anassembled state.

FIG. 44B is a partial cross-sectional view of the vial adaptor of FIG.44A.

FIG. 45 is a perspective view of another embodiment of a housing membercompatible with certain embodiments of the vial adaptor of FIG. 40.

FIG. 46 is a perspective view of another embodiment of a housing membercompatible with certain embodiments of the vial adaptor of FIG. 40.

FIG. 47 is a cross-sectional view of another embodiment of a housingmember compatible with certain embodiments of the vial adaptor of FIG.40.

FIG. 48 is a cross-sectional view of an embodiment of a bag compatiblewith certain embodiments of the housing member of FIG. 47.

FIG. 49 is a cross-sectional view of another embodiment of a housingmember compatible with certain embodiments of the vial adaptor of FIG.40.

DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS

Numerous medicines and other therapeutic fluids are stored anddistributed in medicinal vials of various shapes and sizes. Often, thesevials are hermetically sealed to prevent contamination or leaking of thestored fluid. The pressure differences between the interior of thesealed vials and the particular atmospheric pressure in which the fluidis later removed often give rise to various problems.

For instance, introducing the piercing member of a vial adaptor throughthe septum of a vial can cause the pressure within the vial to risesharply. This pressure increase can cause fluid to leak from the vial atthe interface of the septum and piercing member or at the attachmentinterface of the adaptor and a medical device, such as a syringe. Also,it can be difficult to withdraw an accurate amount of fluid from asealed vial using an empty syringe, or other medical instrument, becausethe fluid may be naturally urged back into the vial once the syringeplunger is released. Furthermore, as the syringe is decoupled from thevial, pressure differences can often cause a small amount of fluid tospurt from either the syringe or the vial. Additionally, in manyinstances, air bubbles are drawn into the syringe as fluid is withdrawnfrom the vial. To rid a syringe of bubbles after removal from the vial,medical professionals often flick the syringe, gathering all bubblesnear the opening of the syringe, and then force the bubbles out. In sodoing, a small amount of liquid usually is expelled from the syringe aswell. Medical personnel generally do not take the extra step tore-couple the syringe with the vial before expelling the bubbles andfluid. In some instances, this may even be prohibited by laws andregulations. Such laws and regulations may also necessitate expellingoverdrawn fluid at some location outside of the vial in certain cases.Moreover, even if extra air or fluid were attempted to be reinserted inthe vial, pressure differences can sometimes lead to inaccuratemeasurements of withdrawn fluid.

To address these problems caused by pressure differentials, medicalprofessionals frequently pre-fill an empty syringe with a precise volumeof ambient air corresponding to the volume of fluid that they intend towithdraw from the vial. The medical professionals then pierce the vialand expel this ambient air into the vial, temporarily increasing thepressure within the vial. When the desired volume of fluid is laterwithdrawn, the pressure differential between the interior of the syringeand the interior of the vial is generally near equilibrium. Smalladjustments of the fluid volume within the syringe can then be made toremove air bubbles without resulting in a demonstrable pressuredifferential between the vial and the syringe. However, a significantdisadvantage to this approach is that ambient air, especially in ahospital setting, may contain various airborne viruses, bacteria, dust,spores, molds, and other unsanitary and harmful debris. The pre-filledambient air in the syringe may contain one or more of these harmfulsubstances, which may then mix with the medicine or other therapeuticfluid in the vial. If this contaminated fluid is injected directly intoa patient's bloodstream, it can be particularly dangerous because itcircumvents many of the body's natural defenses to airborne pathogens.Moreover, patients who need the medicine and other therapeutic fluidsare more likely to be suffering from a diminished infection-fightingcapacity.

In the context of oncology and certain other drugs, all of the foregoingproblems can be especially serious. Such drugs, although helpful wheninjected into the bloodstream of a patient, can be extremely harmful ifinhaled or touched. Accordingly, such drugs can be dangerous if allowedto spurt unpredictably from a vial due to pressure differences.Furthermore, these drugs are often volatile and may instantly aerosolizewhen exposed to ambient air. Accordingly, expelling a small amount ofsuch drugs in order to clear a syringe of bubbles or excess fluid, evenin a controlled manner, is generally not a viable option, especially formedical personnel who may repeat such activities numerous times eachday. Consequently, there is a need for a vial adaptor that reduces theabove-noted problems.

Certain devices exist that allow air to be drawn into a vial as fluid isremoved therefrom. These devices generally use filters. Although filtersremove a large number of contaminants from air as it enters the vial,the filters are not perfect. In some instances the filters arehydrophobic membranes comprising Gortex® or Teflon®. Multiple problemsarise from such assemblies. For example, the hydrophobic nature of thefilters prevents a user from returning overdrawn fluid to the vial. Forexample, in some instances, air is allowed into the vial through achannel as the user withdraws fluid from the vial. However, if the userforces fluid back into the vial, fluid is also forced through thechannel until it contacts the filter. Because the filter is a barrier tofluid, the pressure within the vial will increase as the medicalprofessional continues to force fluid into the vial. As stated above,such pressure increases are prohibited by law in some instances, and inany event, can make it difficult for the user to obtain an accuratedosage. In addition, pressure differences can easily damage the thin anddelicate membranes, causing the filters to occasionally leak and permitharmful liquids to escape.

Furthermore, the use of Gortex® or Teflon® membranes in filtersgenerally requires ethylene oxide (EtO) sterilization, which isexpensive and inconvenient for medical device manufacturers. Preferredalternative methods of sterilization, such as gamma sterilization andelectron beam sterilization, generally ruin such filters. In someinstances, the latter forms of sterilization degrade the Teflon®membranes, making the filters prone to leakage.

In addition, some existing devices are difficult or complicated tocouple with a vial and can require multiple specialized apparatuses toeffectuate such coupling. Complicated procedures can become overlyburdensome to medical personnel who repeat the procedures numerous timeseach day. Furthermore, certain of such complicated devices are bulky andunbalanced. Coupling such a device with a vial generally creates atop-heavy, metastable system that is prone to being tipped over andpossibly spilled.

Disclosed herein are numerous embodiments of vial adaptors that reduceor eliminate many of the above-noted problems.

FIG. 1 is a schematic illustration of a container 10, such as amedicinal vial, that can be coupled with an extractor 20 and a regulator30. In certain arrangements, the regulator 30 allows the removal of someor all of the contents of the container 10 via the extractor 20 withouta significant change of pressure within the container 10.

In general, the container 10 is hermetically sealed to preserve thecontents of the container 10 in a sterile environment. The container 10can be evacuated or pressurized upon sealing. In some instances, thecontainer 10 is partially or completely filled with a liquid, such as adrug or other medical fluid. In such instances, one or more gases canalso be sealed in the container 10. Although embodiments and examplesare provided herein in the medical field, the inventions are notconfined to the medical field only and certain embodiments can be usedin many other fields.

The extractor 20 generally provides access to contents of the container10 such that the contents may be removed or added to. In certainarrangements, the extractor 20 comprises an opening between the interiorand exterior of the container 10. The extractor 20 can further comprisea passageway between the interior and exterior of the container 10. Insome configurations, the passageway of the extractor 20 can beselectively opened and closed. In some arrangements, the extractor 20comprises a conduit extending through a surface of the container 10. Theextractor 20 can be integrally formed with the container 10 prior to thesealing thereof or introduced to the container 10 after the container 10has been sealed.

In some configurations, the extractor 20 is in fluid communication withthe container 10, as indicated by an arrow 21. In certain of theseconfigurations, when the pressure inside the container 10 varies fromthat of the surrounding environment, the introduction of the extractor20 to the container 10 causes a transfer through the extractor 20. Forexample, in some arrangements, the pressure of the environment thatsurrounds the container 10 exceeds the pressure within the container 10,which may cause ambient air from the environment to ingress through theextractor 20 upon insertion of the extractor 20 into the container 10.In other arrangements, the pressure inside the container 10 exceeds thatof the surrounding environment, causing the contents of the container 10to egress through the extractor 20.

In some configurations, the extractor 20 is coupled with an exchangedevice 40. In certain instances, the extractor 20 and the exchangedevice 40 are separable. In some instances, the extractor 20 and theexchange device 40 are integrally formed. The exchange device 40 isconfigured to accept fluids and/or gases from the container 10 via theextractor 20, to introduce fluids and/or gases to the container 10 viathe extractor 20, or to do some combination of the two. In somearrangements, the exchange device 40 is in fluid communication with theextractor 20, as indicated by an arrow 24. In certain configurations,the exchange device 40 comprises a medical instrument, such as asyringe.

In some instances, the exchange device 40 is configured to remove someor all of the contents of the container 10 via the extractor 20. Incertain arrangements, the exchange device 40 can remove the contentsindependent of pressure differences, or lack thereof, between theinterior of the container 10 and the surrounding environment. Forexample, in instances where the pressure outside of the container 10exceeds that within the container 10, an exchange device 40 comprising asyringe can remove the contents of the container 10 if sufficient forceis exerted to extract the plunger from the syringe. The exchange device40 can similarly introduce fluids and/or gases to the container 10independent of pressure differences between the interior of thecontainer 10 and the surrounding environment.

In certain configurations, the regulator 30 is coupled with thecontainer 10. The regulator 30 generally regulates the pressure withinthe container 10. As used herein, the term regulate, or any derivativethereof, is a broad term used in its ordinary sense and includes, unlessotherwise noted, any active, affirmative, or positive activity, or anypassive, reactive, respondent, accommodating, or compensating activitythat tends to effect a change. In some instances, the regulator 30substantially maintains a pressure difference, or equilibrium, betweenthe interior of the container 10 and the surrounding environment. Asused herein, the term maintain, or any derivative thereof, is a broadterm used in its ordinary sense and includes the tendency to preserve anoriginal condition for some period, whether or not that condition isultimately altered. In some instances, the regulator 30 maintains asubstantially constant pressure within the container 10. In certaininstances, the pressure within the container 10 varies by no more thanabout 1 psi, no more than about 2 psi, no more than about 3 psi, no morethan about 4 psi, or no more than about 5 psi. In still furtherinstances, the regulator 30 equalizes pressures exerted on the contentsof the container 10. As used herein, the term equalize, or anyderivative thereof, is a broad term used in its ordinary sense andincludes the movement toward equilibrium, whether or not equilibrium isachieved. In other configurations, the regulator 30 is coupled with thecontainer 10 to allow or encourage equalization of a pressure differencebetween the interior of the container 10 and some other environment,such as the environment surrounding the container 10 or an environmentwithin the exchange device 40. In some arrangements, a single devicecomprises the regulator 30 and the extractor 20, while in otherarrangements, the regulator 30 and the extractor 20 are separate units.

The regulator 30 is generally in communication with the container 10, asindicated by an arrow 31, and a reservoir 50, as indicated by anotherarrow 35. In some configurations, the reservoir 50 comprises at least aportion of the environment surrounding the container 10. In otherconfigurations, the reservoir 50 comprises a container, canister, bag,or other holder dedicated to the regulator 30. As used herein, the termbag is a broad term used in its ordinary sense and includes, withoutlimitation, any sack, balloon, bladder, receptacle, reservoir,enclosure, diaphragm, or membrane capable of expanding and/orcontracting, including structures comprising a flexible, supple,pliable, resilient, elastic, and/or expandable material. In someembodiments, the reservoir 50 comprises a gas and/or a liquid.

In certain embodiments, the regulator 30 provides fluid communicationbetween the container 10 and the reservoir 50. In certain of suchembodiments, it is preferred that the reservoir 50 comprise mainly gasso as not to dilute any liquid contents of the container 10. In somearrangements, the regulator 30 comprises a filter to purify gas orliquid entering the container 10, thereby reducing the risk ofcontaminating the contents of the container 10. In certain arrangements,the filter is hydrophobic such that air can enter the container 10 butfluid cannot escape therefrom.

In other embodiments, the regulator 30 prevents fluid communicationbetween the container 10 and the reservoir 50. In certain of suchembodiments, the regulator 30 serves as an interface between thecontainer 10 and the reservoir 50. In some arrangements, the regulator30 comprises a substantially impervious bag for accommodating ingress ofgas and/or liquid to the container 10 or egress of gas and/or liquidfrom the container 10.

As schematically illustrated in FIG. 2, in certain embodiments, theextractor 20, or some portion thereof, is located within the container10. As detailed above, the extractor 20 can be integrally formed withthe container 10 or separate therefrom. In some embodiments, theregulator 30, or some portion thereof, is located within the container10. In such embodiments, the regulator 30 can be placed in the container10 prior to the sealing thereof or it can be introduced to the container10 thereafter. In some arrangements, the regulator 30 is integrallyformed with the container 10. It is possible to have any combination ofthe extractor 20, or some portion thereof, entirely within, partiallywithin, or outside of the container 10 and/or the regulator 30, or someportion thereof, entirely within, partially within, or outside of thecontainer 10.

In certain embodiments, the extractor 20 is in fluid communication withthe container 10. In further embodiments, the extractor 20 is in fluidcommunication with the exchange device 40, as indicated by the arrow 24.

The regulator 30 can be in fluid or non-fluid communication with thecontainer 10. In some embodiments, the regulator 30 is located entirelywithin the container 10. In certain of such embodiments, the regulator30 comprises a closed bag configured to expand or contract within thecontainer 10 to maintain a substantially constant pressure within thecontainer 10. In other embodiments, the regulator 30 is incommunication, either fluid or non-fluid, with the reservoir 50, asindicated by the arrow 35.

FIG. 3 illustrates an embodiment of a system 100 comprising a vial 110,an extractor 120, and a regulator 130. The vial 110 comprises a body 112and a cap 114. In the illustrated embodiment, the vial 110 contains amedical fluid 116 and a relatively small amount of sterilized air 118.In certain arrangements, the fluid 116 is removed from the vial 110 whenthe vial 110 is oriented with the cap 114 facing downward (i.e., the cap114 is between the fluid and the ground). The extractor 120 comprises aconduit 122 fluidly connected at one end to an exchange device 140,which comprises a standard syringe 142 with a plunger 144. The conduit122 extends through the cap 114 and into the fluid 116. The regulator130 comprises a bag 132 and a conduit 134. The bag 132 and the conduit134 are in fluid communication with a reservoir 150, which comprises theambient air surrounding both the system 100 and the exchange device 140.The bag 132 comprises a substantially impervious material such that thefluid 116 and the air 118 inside the vial 110 do not contact the ambientair located at the interior of the bag 132.

In the illustrated embodiment, areas outside of the vial 110 are atatmospheric pressure. Accordingly, the pressure on the syringe plunger144 is equal to the pressure on the interior of the bag 132, and thesystem 100 is in equilibrium. The plunger 144 can be withdrawn to fillthe syringe 142 with the fluid 116. Withdrawing the plunger 144increases the effective volume of the vial 110, thereby decreasing thepressure within the vial 110. A decrease of pressure within the vial 110increases the difference in pressure between the interior and exteriorof the bag 132, which causes the bag 132 to expand and force fluid intothe syringe 142. In effect, the bag 132 expands within the vial 110 to anew volume that compensates for the volume of the fluid 116 withdrawnfrom the vial 110. Thus, once the plunger 144 ceases from beingwithdrawn from the vial 110, the system is again in equilibrium.Advantageously, the system 100 operates near equilibrium, facilitatingwithdrawal of the fluid 116. Furthermore, due to the equilibrium of thesystem 100, the plunger 144 remains at the position to which it iswithdrawn, thereby allowing removal of an accurate amount of the fluid116 from the vial 110.

In certain arrangements, the increased volume of the bag 132 isapproximately equal to the volume of liquid removed from the vial 110.In some arrangements, the volume of the bag 132 increases at a slowerrate as greater amounts of fluid are withdrawn from the vial 110 suchthat the volume of fluid withdrawn from the vial 110 is greater than theincreased volume of the bag 132.

In some arrangements, the bag 132 can stretch to expand beyond a restingvolume. In some instances, the stretching gives rise to a restorativeforce that effectively creates a difference in pressure between theinside of the bag 132 and the inside of the vial 110. For example, aslight vacuum inside the vial 110 can be created when the bag 132 isstretched.

In certain instances, more of the fluid 116 than desired initially mightbe withdrawn inadvertently. In other instances, some of the air 118 inthe vial 110 initially might be withdrawn, creating unwanted bubbleswithin the syringe 142. It may thus be desirable to inject some of thewithdrawn fluid 116 and/or air 118 back into the vial 110, which can beaccomplished by depressing the plunger 144. Depressing the plunger 144increases the pressure inside the vial 110 and causes the bag 132 tocontract. When the manual force applied to the plunger 144 ceases, theplunger is again exposed to atmospheric pressure alone, as is theinterior of the bag 132. Accordingly, the system 100 is again atequilibrium. Because the system 100 operates near equilibrium as thefluid 116 and/or the air 118 are injected into the vial 110, thepressure within the vial 110 does not significantly increase as thefluid 116 and/or air 118 is returned to the vial 110.

FIG. 4 illustrates an embodiment of a vial adaptor 200 for coupling witha vial 210. The vial 210 can comprise any suitable container for storingmedical fluids. In some instances, the vial 210 comprises any of anumber of standard medical vials known in the art, such as thoseproduced by Abbott Laboratories of Abbott Park, Ill. Preferably, thevial 210 is capable of being hermetically sealed. In someconfigurations, the vial 210 comprises a body 212 and a cap 214. Thebody 212 preferably comprises a rigid, substantially imperviousmaterial, such as plastic or glass. In some embodiments, the cap 214comprises a septum 216 and a casing 218. The septum 216 can comprise anelastomeric material capable of deforming in such a way when puncturedby an item that it forms a substantially airtight seal around that item.For example, in some instances, the septum 216 comprises silicone rubberor butyl rubber. The casing 218 can comprise any suitable material forsealing the vial 210. In some instances, the casing 218 comprises metalthat is crimped around the septum 216 and a proximal portion of the body212 in order to form a substantially airtight seal between the septum216 and the vial 210. In certain embodiments, the cap 214 defines ridge219 that extends outwardly from the top of the body 212.

In certain embodiments, the adaptor 200 comprises a piercing member 220.In some configurations, the piercing member 220 comprises a sheath 222.The sheath 222 can be substantially cylindrical, as shown, or it canassume other geometric configurations. In some instances, the sheath 222tapers toward a distal end 223. In some arrangements, the distal end 223defines a point that can be centered with respect to an axis of thepiercing member 220 or offset therefrom. In certain embodiments, thedistal end 223 is angled from one side of the sheath 222 to the oppositeside. The sheath 222 can comprise a rigid material, such as metal orplastic, suitable for insertion through the septum 216. In certainembodiments the sheath 222 comprises polycarbonate plastic.

In some configurations, the piercing member 220 comprises a tip 224. Thetip 224 can have a variety of shapes and configurations. In someinstances, the tip 224 is configured to facilitate insertion of thesheath 222 through the septum 216. As illustrated, the tip 224, or aportion thereof, can be substantially conical, coming to a point at ornear the axial center of the piercing member 220. In someconfigurations, the tip 224 angles from one side of the piercing member220 to the other. In some instances, the tip 224 is separable from thesheath 222. In other instances, the tip 224 and the sheath 222 arepermanently joined, and can be integrally formed. In variousembodiments, the tip 224 comprises acrylic plastic, ABS plastic, orpolycarbonate plastic.

In some embodiments, the adaptor 200 comprises a cap connector 230. Asillustrated, the cap connector 230 can substantially conform to theshape of the cap 214. In certain configurations, the cap connector 230comprises a rigid material, such as plastic or metal, that substantiallymaintains its shape after minor deformations. In some embodiments, thecap connector 230 comprises polycarbonate plastic. In some arrangements,the cap connector 230 comprises a sleeve 235 configured to snap over theridge 219 and tightly engage the cap 214. As more fully described below,in some instances, the cap connector 230 comprises a material around aninterior surface of the sleeve 235 for forming a substantially airtightseal with the cap 214. In some embodiments, the cap connector 230comprises an elastic material that is stretched over the ridge 219 toform a seal around the cap 214. In some embodiments, the cap connector230 resembles the structures shown in FIGS. 6 and 7 of and described inthe specification of U.S. Pat. No. 5,685,866, the entire contents ofwhich are hereby incorporated by reference herein and are made a part ofthis specification.

In certain embodiments, the adaptor 200 comprises a medical connectorinterface 240 for coupling the adaptor 200 with a medical connector 241,another medical device (not shown), or any other instrument used inextracting fluid from or injecting fluid into the vial 210. In certainembodiments, the medical connector interface 240 comprises a sidewall248 that defines a proximal portion of an extractor channel 245 throughwhich fluid may flow. In some instances, the extractor channel 245extends through the cap connector 230 and through a portion of thepiercing member 220 such that the medical connector interface 240 is influid communication with the piercing member 220. The sidewall 248 canassume any suitable configuration for coupling with the medicalconnector 241, a medical device, or another instrument. In theillustrated embodiment, the sidewall 248 is substantially cylindricaland extends generally proximally from the cap connector 230.

In certain configurations, the medical connector interface 240 comprisesa flange 247 to aid in coupling the adaptor 200 with the medicalconnector 241, a medical device, or another instrument. The flange 247can be configured to accept any suitable medical connector 241,including connectors capable of sealing upon removal of a medical devicetherefrom. In some instances, the flange 247 is sized and configured toaccept the Clave® connector, available from ICU Medical, Inc. of SanClemente, Calif. Certain features of the Clave® connector are disclosedin U.S. Pat. No. 5,685,866. Connectors of many other varieties,including other needle-less connectors, can also be used. The connector241 can be permanently or separably attached to the medical connectorinterface 240. In other arrangements, the flange 247 is threaded,configured to accept a Luer connector, or otherwise shaped to attachdirectly to a medical device, such as a syringe, or to otherinstruments.

In certain embodiments, the medical connector interface 240 isadvantageously centered on an axial center of the adaptor 200. Such aconfiguration provides stability to a system comprising the adaptor 200coupled with the vial 210, thereby making the coupled system less likelyto tip over. Accordingly, the adaptor 200 is less likely to causedangerous leaks or spills occasioned by accidental bumping or tipping ofthe adaptor 200 or the vial 210.

In some embodiments, the piercing member 220, the cap connector 230, andthe medical connector interface 240 are integrally formed of a unitarypiece of material, such as polycarbonate plastic. In other embodiments,one or more of the piercing member 220, the cap connector 230, and themedical connector interface 240 comprise a separate piece. The separatepieces can be joined in any suitable manner, such as by glue, epoxy,ultrasonic welding, etc. Preferably, connections between joined piecescreate substantially airtight bonds between the pieces. In furtherarrangements, any of the piercing member 220, the cap connector 230, orthe medical connector interface 240 can comprise more than one piece.

In certain embodiments, the adaptor 200 comprises a regulator aperture250. In many embodiments, the regulator aperture 250 is located at aposition on the adaptor 200 that remains exposed to the exterior of thevial 210 when the piercing member 220 is inserted in the vial 210. Inthe illustrated embodiment, the regulator aperture 250 is located at ajunction of the cap connector 230 and the medical connector interface240. In certain embodiments, the regulator aperture 250 allows fluidcommunication between the environment surrounding the vial 210 and aregulator channel 225 (see FIG. 5) which extends through the capconnector 230 and through the piercing member 220.

FIG. 5 illustrates a cross-section of the vial adaptor 200 coupled withthe vial 210. In the illustrated embodiment, the cap connector 230firmly secures the adaptor 200 to the cap 214 and the piercing member220 extends through the septum 216 into the interior of the vial 210. Insome embodiments, the piercing member 220 is oriented substantiallyperpendicularly with respect to the cap 214 when the adaptor 200 and thevial 210 are coupled. Other configurations are also possible. As shown,in some embodiments, the piercing member 220 houses a bag 260.

In certain embodiments, the cap connector 230 comprises one or moreprojections 237 that aid in securing the adaptor 200 to the vial 210.The one or more projections 237 extend toward an axial center of the capconnector 230. In some configurations, the one or more projections 337comprise a single circular flange extending around the interior of thecap connector 330. The cap connector 230 can be sized and configuredsuch that an upper surface of the one or more projections 237 abuts alower surface of the ridge 219, helping secure the adaptor 200 in place.

The one or more projections 237 can be rounded, chamfered, or otherwiseshaped to facilitate the coupling of the adaptor 200 and the vial 210.For example, as the adaptor 200 having rounded projections 237 isintroduced to the vial 210, a lower surface of the rounded projections237 abuts a top surface of the cap 214. As the adaptor 200 is advancedonto the vial 210, the rounded surfaces cause the cap connector 230 toexpand radially outward. As the adaptor 200 is advanced further onto thevial 210, a resilient force of the deformed cap connector 220 seats theone or more projections 237 under the ridge 219, securing the adaptor200 in place.

In some embodiments, the cap connector 230 is sized and configured suchthat an inner surface 238 of the cap connector 230 contacts the cap 214.In some embodiments, a portion of the cap connector 230 contacts the cap214 in substantially airtight engagement. In certain embodiments, aportion of the inner surface 238 surrounding either the septum 216 orthe casing 218 is lined with a material, such as rubber or plastic, toensure the formation of a substantially airtight seal between theadaptor 200 and the vial 210.

The piercing member 220 can comprise the tip 224 and the sheath 222, asnoted above. In some embodiments, the tip 224 is configured to piercethe septum 216 to facilitate passage therethrough of the sheath 222. Insome instances, the tip 224 comprises a proximal extension 224 a forsecuring the tip 224 to the sheath 222. As described below, in somearrangements, the bag 260 is folded within the sheath 222. Accordingly,a portion of the folded bag 260 can contact the proximal extension 224 aand hold it in place. In many arrangements, the proximal extension 224 acomprises a material capable of frictionally engaging the bag 260. Invarious embodiments, the proximal extension 224 a comprisespolycarbonate plastic, silicone rubber, butyl rubber, or closed cellfoam. In some arrangements, the proximal extension 224 a is coated withan adhesive to engage the bag 260. The proximal extension 224 a can beattached to the tip 224 by any suitable means, or it can be integrallyformed therewith.

In some arrangements, the tip 224 can be adhered to, friction fitwithin, snapped into, or otherwise attached in a temporary fashion tothe distal end 223 of the sheath 222, either instead of or in additionto any engagement between the proximal extension 224 a and the bag 260.As discussed below, in some arrangements, the tip 224 disengages fromthe sheath 222 and/or the bag 260 as fluid is withdrawn from the vial210. In other arrangements, the tip 224 disengages from the sheath 222and/or the bag 260 upon passing through the septum 216, such as whenatmospheric pressure within the sheath 222 is sufficiently higher thanthe pressure within the vial 210. In other instances, a volume of airbetween the tip 224 and the bag 260 is pressurized to achieve the sameresult.

In some embodiments, the tip 224 comprises a shoulder 224 b. In someinstances, the outer perimeter of the shoulder 224 b is shaped toconform to the interior perimeter of the sheath 222. Accordingly, theshoulder 224 b can center the tip 224 with respect to the sheath 222 andkeep the tip 224 oriented properly for insertion through the septum 216.In some instances, the outer perimeter of the shoulder 224 b is slightlysmaller than the interior perimeter of the sheath 222, allowing the tip224 to easily disengage or slide from the sheath 222 as the bag 260 isdeployed. In certain embodiments, the tip 224 comprises the shoulder 224b, but does not comprise the proximal extension 224 a.

In certain arrangements, the proximal extension 224 a serves to maintaina proper orientation of the tip 224 with respect to the sheath 222 forinsertion of the tip 224 through the septum 216. In some instances, thetip 224 rotates with respect to the sheath 222 as the tip 224 contactsthe septum 216 such that the proximal extension 224 a is angled withrespect to the axial center of the sheath 222. In some arrangements, theproximal extension 224 a is sufficiently long that an end thereofcontacts the interior surface of the sheath 222. In many instances, thecontact is indirect, where one or more layers of the bag 260 are locatedbetween the proximal extension 224 a and the sheath 222. This contactcan prevent the tip 224 from rotating too far, such that a distal end224 c thereof is not directed at an angle that is relativelyperpendicular to the septum 216.

The sheath 222 is generally sized and dimensioned to be inserted throughthe septum 216 without breaking and, in some instances, with relativeease. Accordingly, in various embodiments, the sheath 222 has across-sectional area of between about 0.025 and about 0.075 squareinches, between about 0.040 and about 0.060 square inches, or betweenabout 0.045 and about 0.055 square inches. In other embodiments, thecross-sectional area is less than about 0.075 square inches, less thanabout 0.060 square inches, or less than about 0.055 square inches. Instill other embodiments, the cross-sectional area is greater than about0.025 square inches, greater than about 0.035 square inches, or greaterthan about 0.045 square inches. In some embodiments, the cross-sectionalarea is about 0.050 square inches.

The sheath 222 can assume any of a number of cross-sectional geometries,such as, for example, oval, ellipsoidal, square, rectangular, hexagonal,or diamond-shaped. The cross-sectional geometry of the sheath 222 canvary along a length thereof in size and/or shape. In some embodiments,the sheath 222 has substantially circular cross-sections along asubstantial portion of a length thereof. A circular geometry providesthe sheath 222 with substantially equal strength in all radialdirections, thereby preventing bending or breaking that might otherwiseoccur upon insertion of the sheath 222. The symmetry of an openingcreated in the septum 216 by the circular sheath 222 prevents pinchingthat might occur with angled geometries, allowing the sheath 222 to moreeasily be inserted through the septum 216. Advantageously, the matchingcircular symmetries of the piercing member 220 and the opening in theseptum 216 ensure a tight fit between the piercing member 220 and theseptum 216, even if the adaptor 200 is inadvertently twisted.Accordingly, the risk of dangerous liquids or gases escaping the vial210, or of impure air entering the vial 210 and contaminating thecontents thereof, can be reduced in some instances with a circularlysymmetric configuration.

In some embodiments, the sheath 222 is hollow. In the illustratedembodiment, the inner and outer surfaces of the sheath 222 substantiallyconform to each other such that the sheath 222 has a substantiallyuniform thickness. In various embodiments, the thickness is betweenabout 0.015 inches and 0.040 inches, between about 0.020 inches and0.030 inches, or between about 0.024 inches and about 0.026 inches. Inother embodiments, the thickness is greater than about 0.015 inches,greater than about 0.020 inches, or greater than about 0.025 inches. Instill other embodiments, the thickness is less than about 0.040 inches,less than about 0.035 inches, or less than about 0.030 inches. In someembodiments, the thickness is about 0.025 inches.

In other embodiments, the inner surface of the sheath 222 varies inconfiguration from that of the outer surface of the sheath 222.Accordingly, in some arrangements, the thickness varies along the lengthof the sheath 222. In various embodiments, the thickness at one end,such as a proximal end, of the sheath is between about 0.015 inches andabout 0.050 inches, between about 0.020 inches and about 0.040 inches,or between about 0.025 inches and about 0.035 inches, and the thicknessat another end, such as the distal end 223, is between about 0.015inches and 0.040 inches, between about 0.020 inches and 0.030 inches, orbetween about 0.023 inches and about 0.027 inches. In other embodiments,the thickness at one end of the sheath 222 is greater than about 0.015inches, greater than about 0.020 inches, or greater than about 0.025inches, and the thickness at another end thereof is greater than about0.015 inches, greater than about 0.020 inches, or greater than about0.025 inches. In still other embodiments, the thickness at one end ofthe sheath 222 is less than about 0.050 inches, less than about 0.040inches, or less than about 0.035 inches, and the thickness at anotherend thereof is less than about 0.045 inches, less than about 0.035inches, or less than about 0.030 inches. In some embodiments, thethickness at a proximal end of the sheath 222 is about 0.030 inches andthe thickness at the distal end 223 is about 0.025 inches. In somearrangements, the cross-section of the inner surface of the sheath 222is shaped differently from that of the outer surface. The shape andthickness of the sheath 222 can be altered to optimize the strength ofthe sheath 222.

In some instances the length of the sheath 222, as measured from adistal surface of the cap connector 230 to the distal end 223 is betweenabout 0.8 inches to about 1.4 inches, between about 0.9 inches and about1.3 inches, or between about 1.0 inches and 1.2 inches. In otherinstances the length is greater than about 0.8 inches, greater thanabout 0.9 inches, or greater than about 1.0 inches. In still otherinstances, the length is less than about 1.4 inches, less than about 1.3inches, or less than about 1.2 inches. In some embodiments, the lengthis about 1.1 inches.

In certain embodiments, the sheath 222 at least partially encloses oneor more channels. In the illustrated embodiment, the sheath 222 definesthe outer boundary of a distal portion of a regulator channel 225 andthe outer boundary of a distal portion of the extractor channel 245. Aninner wall 227 extending from an inner surface of the sheath 222 to adistal portion of the medical connector interface 240 defines an innerboundary between the regulator channel 225 and the extractor channel245. The regulator channel 225 extends from a proximal end 262 of thebag 260, through the cap connector 230, between the cap connector 230and the medical connector interface 240, and terminates at a regulatoraperture 250. The extractor channel 245 extends from an extractoraperture 246 formed in the sheath 222, through the cap connector 230,and through the medical connector interface 240.

In certain embodiments, the sheath 222 contains the bag 260. The bag 260is generally configured to unfold, expand, compress, and/or contract,and can comprise any of a wide variety of materials, including Mylar®,polyester, polyethylene, polypropylene, saran, latex rubber,polyisoprene, silicone rubber, and polyurethane. In some embodiments,the bag 260 comprises a material capable of forming a substantiallyairtight seal with the sheath 222. In other embodiments, the bag 260comprises a material that can be adhered to the sheath 222 insubstantially airtight engagement. In many instances, the bag 260comprises a material that is generally impervious to liquid and air. Incertain embodiments, it is preferred that the bag 260 comprise amaterial that is inert with respect to the intended contents of the vial210. In some embodiments, the bag 260 comprises latex-free siliconehaving a durometer between about 10 and about 40.

In some configurations, at least the proximal end 262 of the bag 260 isin substantially airtight engagement with the sheath 222. In someinstances, such as that of the illustrated embodiment, a substantiallyairtight seal is achieved when the proximal end 262 is thicker thanother portions of the bag 260 and fits more snugly within the sheath 222than the remainder of the bag 260. In certain instances, the thickerproximal end 262 comprises a higher durometer material than theremainder of the bag 260. In some instances, the proximal end 262comprises latex-free silicone having a durometer between about 40 andabout 70. In other instances, the proximal end 262 is retained in thesheath 222 by a plastic sleeve (not shown) that presses the proximal end262 against the sheath 222. In still further instances, the proximal end262 is adhered to the sheath 222 by any suitable manner, such as by heatsealing or gluing. In some embodiments, a greater portion of the bag 260than just the proximal end 262 is in substantially airtight contact withthe sheath 222.

In certain embodiments, the proximal end 262 of the bag 260 defines abag aperture 264. In some instances, the bag aperture 264 allows fluidcommunication between the interior of the bag 260 and the regulatorchannel 225. In certain arrangements, the bag aperture 264 extends alongan axial center of the proximal end 262. Accordingly, in certain of sucharrangements, a lower portion of the interior wall 227 is angled (asshown), offset, or positioned away from the center of the sheath 222 soas not to obstruct the bag aperture 264.

In certain arrangements, the entire bag 260 is located within the sheath222 prior to insertion of the adaptor 200 into the vial 210.Accordingly, the bag 260 is generally protected by the sheath 222 fromrips or tears when the adaptor 200 is inserted in the vial 210. In someinstances, a lubricant is applied to an outer surface of the bag 260 tofacilitate the insertion thereof into the sheath 222. As used herein,the term “lubricant” is a broad term used in its ordinary sense andincludes, without limitation, any substance or material used to permitsubstantially unimpeded relative movement of surfaces in closeproximity, including, without limitation: gels, liquids, powders, and/orcoatings applied to one or more of the surfaces; materials, compounds,or substances embedded within one or more of the surfaces; andsubstances or materials placed between the surfaces. In someembodiments, the lubricant is a liquid, a gel, or a powder. In certainembodiments, the lubricant applied to the outer surface of the bag 260is isopropyl alcohol, which desirably is sterile, readily evaporates,and provides sufficient lubrication to allow relatively simple insertionof the bag 260. Other lubricants having the same or different propertiescan also be employed.

In the illustrated embodiment, a portion of the bag 260 is internallyfolded or doubled back within the sheath 222. In certain embodiments,the bag 260 comprises a material that does not readily cling to itself,thereby allowing portions of the bag 260 in close proximity (e.g.,adjacent to each other) to slide past each other and away from eachother with relative ease, thus allowing the bag 260 to be deployedeasily. In some embodiments, a lubricant is applied to the interiorsurface of the bag 260 to encourage a relatively unimpeded deployment ofthe bag 260. Any suitable variety of lubricant is possible. In someembodiments, the lubricant comprises a liquid or a gel. In someembodiments, the lubricant comprises fluorosilicone oil. In otherembodiments, the lubricant comprises a powder, such as talcum powder. Insome embodiments, powder lubricants are more effective than liquid orgel lubricants over extended storage periods. For example, certainliquids and gels can migrate from between two proximate surfaces of thebag 260, whereas certain powders can be less prone to migrate therefrom.Accordingly, in some embodiments, some powder lubricants can provide anadaptor 200 with a relatively longer shelf-life than some liquid or gellubricants. In other embodiments, liquids (e.g., oils) are preferred.

In further embodiments, the lubricant comprises a coating that isadhered to, integrally formed with, or otherwise applied to the bag 260.The coating can comprise any suitable material that can permitrelatively unimpeded movement between surfaces of the bag 260. Forexample, some embodiments can comprise a coating of friction-reducingmaterial, such as Teflon®. In still further embodiments, the lubricantis embedded in the bag 260

In some embodiments, one or more portions of the bag 260 are foldedmultiple times within the sheath 222. In certain of such embodiments, alubricant can be applied to portions of the interior and/or exteriorsurfaces of the bag 260 to allow relatively easy deployment of the bag260.

FIGS. 6A and 6B schematically illustrate why it can be desirable to foldthe bag 260 within the sheath 222 in some instances. FIG. 6A illustratesa distal portion of the sheath 222 of the adaptor 200. The sheath 222houses a substantially impervious bag 260A comprising a proximal portion266A and a tip 269A. The adaptor 200 is coupled with a partiallyevacuated vial 210 (not shown) such that the pressure outside the vial210 (e.g., atmospheric pressure) is higher than the pressure inside thevial 210. Accordingly, one side of the bag 260A can be exposed to thehigher pressure outside the vial 210 and the other side of the bag 260Acan be exposed to the lower pressure inside the vial 210. As a result ofthe pressure difference, the proximal portion 266A of the bag 260A isforced toward the inner surface of the sheath 222, as schematicallydepicted by various arrows. The friction thus generated tends to preventthe proximal portion 266A from expanding toward the distal end of thesheath 222. Consequently, in the illustrated configuration, only the tip269A is able to expand when fluid is withdrawn from the vial 210.Withdrawing a large amount of fluid could put excessive strain on thetip 269A, causing it to tear or burst. In some embodiments, thecomposition of the bag 260A and/or the interface between the bag 260Aand the interior wall of the sheath 222 permit much further expansion ofthe bag 260A in the distal direction.

FIG. 6B similarly illustrates a distal portion of the sheath 222 housinga substantially impervious bag 260B. The bag 260B comprises an outerportion 266B, an inner portion 268B, and a tip 269B. As in FIG. 6A, theadaptor 200 is coupled with a partially evacuated vial 210 such that thepressure outside the vial 210 is higher than the pressure inside thevial 210. The resulting pressure difference forces the outer portion266B toward the sheath 222, as schematically depicted by variousoutward-pointing arrows. However, the pressure difference forces theinner portion 268B toward the center of the sheath 222, as schematicallydepicted by various inward-pointing arrows. As a result, frictionbetween the inner portion 268B and the outer portion 266B of the bag260B is reduced or eliminated, thereby facilitating expansion of theinner portion 268B and of the tip 269B toward and through the distal end223 of the sheath 222. Consequently, in the illustrated embodiment, alarger portion of the bag 260B than that of the bag 260A is able toexpand within the vial 210.

FIG. 7 illustrates an embodiment of the adaptor 200 with the bag 260deployed. As shown, in some embodiments, a distal portion 268 of the bag260 extends beyond the sheath 222. In certain arrangements, a portion ofthe bag 260 that contacts the distal end 223 of the sheath 222 isthicker than surrounding portions in order to protect the bag 260 fromripping, puncturing, or tearing against the sheath 222.

In some embodiments, the bag 260 is sized and configured tosubstantially fill the vial 210. For example, in some arrangements, thebag 260 comprises a flexible, expandable material sized and configuredto expand to fill a substantial portion of the volume within the vial210. In some instances, the bag 260 is expandable to substantially filla range of volumes such that a single adaptor 200 can be configured tooperate with vials 210 of various sizes. In other arrangements, the bag260 comprises a flexible, non-expandable material and is configured tounfold within the vial 210 to fill a portion thereof. In someembodiments, the bag 260 is configured to fill at least about 25, 30,35, 40, 45, 50, 60, 70, 80, or 90 percent of one vial 210. In otherembodiments, the bag 260 is configured to fill a volume equal to atleast about 30, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, or 90 percent ofthe volume of fluid contained within the vial 210 prior to the couplingof the adaptor 200 and the vial 210. In some embodiments, the bag 260 isconfigured to fill a volume equal to about 70 percent of the volume offluid contained within the vial 210 prior to the coupling of the adaptor200 and the vial 210. In other embodiments, the bag 260 is configured tofill at least about 25, 30, 35, 40, 45, 50, 60, 70, 80, or 90 percent ofa first vial 210 having a first volume, and at least about 25, 30, 35,40, 45, 50, 60, 70, 80, or 90 percent of a second vial 210 having asecond volume larger than the first volume.

In some configurations, the distal portion 268 of the bag 260 issubstantially bulbous, as shown. In some embodiments, the bulbous bag260 comprises expandable material. In various arrangements, the distalportion 268 in an unexpanded state has an outer diameter of betweenabout 0.10 inches and about 0.40 inches, between about 0.15 inches andabout 0.35 inches, or between about 0.20 inches and about 0.30 inches.In some arrangements, the outer diameter is greater than about 0.10,greater than about 0.15 inches, or greater than about 0.20 inches. Inother arrangements, the outer diameter is less than about 0.40 inches,less than about 0.35 inches, or less than about 0.30 inches. In somearrangements, the outer diameter is about 0.188 inches. In variousarrangements, the distal portion 268 in an unexpanded state has a heightof between about 0.50 inches and 1.00 inches, between about 0.60 inchesand 0.90 inches, and between about 0.70 inches and 0.80 inches. In somearrangements, the height is greater than about 0.50 inches, greater thanabout 0.60 inches, or greater than about 0.70 inches. In otherarrangements, the height is less than about 1.00 inches, less than about0.90 inches, or less than about 0.80 inches. In some arrangements, theheight is about 0.75 inches. In some embodiments, the distal portion isgenerally spherical. Various other embodiments of the distal portion 268include, for example, generally conical, generally cylindrical,generally rectangular, and generally triangular.

In some configurations, the distal portion 268 of the bag 260 has athickness between about 0.001 and 0.025 inches, between about 0.001 and0.010 inches, or between about 0.010 and 0.025 inches. In otherconfigurations, the thickness is greater than about 0.001 inches,greater than about 0.005 inches, greater than about 0.010 inches,greater than about 0.015 inches, or greater than about 0.020 inches. Instill other configurations, the thickness is less than about 0.025inches, less than about 0.020 inches, less than about 0.015 inches, lessthan about 0.010 inches, or less than about 0.005 inches. In someconfigurations, the thickness is about 0.015 inches.

As noted above, in some instances the body 212 of the vial 210 comprisesa substantially rigid material, such as glass or plastic. Accordingly,configurations wherein the bag 260 is deployed within the vial 210advantageously shield the bag 260 from accidental snags, rips, or tears.Furthermore, configurations wherein the bag 260 is located within thevial 210 can have a lower center of mass than other configurations,which helps to prevent accidental tipping and spilling of the vial 210.

With continued reference to FIG. 7, certain processes for using theadaptor 200 comprise inserting the piercing member 220 through theseptum 216 until the cap connector 230 is firmly in place. Accordingly,the coupling of the adaptor 200 and the vial 210 can be accomplished inone simple step. In certain instances, the medical connector 241 iscoupled with the medical connector interface 240. A medical device orother instrument (not shown), such as a syringe, can be coupled with theinterface 240 or, if present, with the medical connector 241 (see FIG.4). For convenience, reference will be made hereafter only to a syringeas an example of a medical device suitable for attachment to the medicalconnector interface 240, although numerous medical devices or otherinstruments can be used in connection with the adaptor 200 or themedical connector 241. In some instances, the syringe is placed in fluidcommunication with the vial 210. In some instances, the vial 210, theadaptor 200, the syringe, and, if present, the medical connector 241 areinverted such that the cap 214 is pointing downward (i.e., toward theground). Any of the above procedures, or any combination thereof, can beperformed in any possible order.

In some instances, a volume of fluid is withdrawn from the vial 210 viathe syringe. As described above, the pressure within the vial 210decreases as the fluid is withdrawn. Accordingly, in some instances,pressure within the regulator channel 225 forces the tip 224 away fromthe sheath 222. In other instances, pressure at the interior of the bag260 causes the bag 260 to emerge from the sheath 222. In certain of suchinstances, as the bag 260 is deployed, it rolls outward and releases theproximal extension 224 a, thus discharging the tip 224. The bag 260 isthus free to expand within the vial 210. In certain arrangements,therefore, it is desirable for the tip 224 to be engaged with the sheath222 and/or bag 260 with sufficient strength to ensure that the tip 224remains in place until the sheath 222 is inserted into the vial 210, yetwith insufficient strength to prevent the tip 224 from separating fromthe sheath 222 and/or the bag 260 within the vial 210.

In some embodiments, the distal end 224 c of the tip 224 is rounded suchthat it is sufficiently pointed to pierce the septum 216 when theadaptor 200 is coupled with the vial 210, but insufficiently pointed topierce the bag 260 as the bag 260 is deployed or as it expands withinthe vial 210. In some arrangements, the proximal extension 224 a isrounded for the same purpose.

In some instances, it is desirable to prevent the bag 260 from bearingagainst the distal end 224 c of the tip 224 as the bag 260 expandswithin the vial 210. Accordingly, in certain arrangements, the proximalextension 224 a is configured such that the tip 224, once separated fromthe sheath 222, naturally settles with the distal end 224 c pointed awayfrom the bag 260. For example, in some instances, the distal end 224 csettles against the septum 216 when the vial 210 is oriented with thecap 214 pointing downward (i.e., with the cap 214 located between avolumetric center of the vial 210 and the ground). In some arrangements,the proximal extension 224 a is relatively lightweight such that thecenter of mass of the tip 224 is located relatively near the distal end224 c. Accordingly, in some instances, when the tip 224 contacts theseptum 216, the tip 224 is generally able to pivot about an edge 224 dto reach a stable state with the distal end 224 c pointed downward. Insome arrangements, the edge 224 d comprises the perimeter of the largestcross-section of the tip 224.

In certain embodiments, the proximal extension 224 a is configured toallow the tip 224 to pivot such that the distal end 224 c ultimatelypoints downward, even when the proximal extension 224 a is pointeddownward upon initial contact with some surface of the vial 210, such asthe septum 216. In certain instances, the length and/or weight of theproximal extension 224 a are adjusted to achieve this result. In someinstances, the length of the proximal extension 224 a is between about30 percent and about 60 percent, between about 35 percent and about 55percent, or between about 40 percent and about 50 percent of the fulllength of the tip 224. In certain embodiments, the length of theproximal extension 224 a is less than about 60 percent, less than about55 percent, or less than about 50 percent of the full length of the tip224. In other embodiments, the length is greater than about 60 percentof the full length of the tip 224. In still other embodiments, thelength is less than about 30 percent of the full length of the tip 224.In some embodiments, the length is about 45 percent of the full lengthof the tip 224. Other arrangements are also possible to ensure that thedistal end 224 c does not bear against the bag 260 as the bag expandswithin the vial 210.

In some arrangements, it is also desirable that the proximal extension224 a not rigidly bear against the bag 260 as the bag 260 expands withinthe vial 210. Accordingly, in some embodiments, the proximal extension224 a comprises a flexible or compliant material, such as siliconerubber, butyl rubber, or closed cell foam. In other embodiments, theproximal extension 224 a comprises a joint, such as a hinge or aball-and-socket, that allows the proximal extension 224 a to bend whencontacted by the bag 260.

In certain configurations, fluid withdrawn from the vial 210 flowsthrough the extractor aperture 246 and through the extractor channel 245to the syringe. Simultaneously, in such configurations, ambient airflows from the surrounding environment, through the regulator aperture250, through the regulator channel 225, through the bag aperture 264,and into the bag 260 to expand the bag 260. In certain arrangements, theincreased volume of the bag 260 is approximately equal to the volume ofliquid removed from the vial 210. In other arrangements, the volume ofthe bag 260 increases at a slower rate as greater amounts of fluid arewithdrawn from the vial 210 such that the volume of fluid withdrawn fromthe vial 210 is greater than the increased volume of the bag 260. Asnoted above, the bag 260 can be configured to fill a substantial portionof the vial 210. In some configurations, the tip 224 is sized andconfigured such that it will not settle against the extractor aperture246 and prevent fluid passage therethrough.

In some instances, more fluid than is desired may inadvertently bewithdrawn from the vial 210 by the syringe. Accordingly, the excessfluid may be injected from the syringe back into the vial 210. In someconfigurations, when the fluid is injected to the vial 210, the fluidflows from the syringe, through the extractor channel 245, and throughthe extractor aperture 246 into the vial 210. As the fluid is forcedinto the vial 210, the pressure within the vial 210 increases.Consequently, in some configurations, the bag 260 contracts to a smallervolume to compensate for the volume of the returned fluid. As the bag260 contracts, ambient air flows from the bag 260, through the bagaperture 264, through the regulator channel 225, and through theregulator aperture 250 to the surrounding environment, in somearrangements.

Thus, in certain embodiments, the adaptor 200 accommodates thewithdrawal of fluid from, or the addition of fluid to, the vial 210 inorder to maintain the pressure within the vial 210. In variousinstances, the pressure within the vial 210 changes no more than about 1psi, no more than about 2 psi, no more than about 3 psi, no more thanabout 4 psi, or no more than about 5 psi.

As is evident from the embodiments and processes described above, theadaptor 200 advantageously allows a user to return unwanted liquid(and/or air) to the vial 210 without significantly increasing thepressure within the vial 210. As detailed earlier, the ability to injectair bubbles and excess fluid into the vial 210 is particularly desirablein the context of oncology drugs.

Furthermore, the above discussion demonstrates that certain embodimentsof the adaptor 200 are configured to regulate the pressure within thevial 210 without introducing outside air into the vial 210. For example,in some embodiments, the bag 260 comprises a substantially imperviousmaterial that serves as a barrier, rather than a passageway, between theexterior and interior of the vial 210. Accordingly, such embodiments ofthe adaptor 200 substantially reduce the risk of introducing airbornecontaminants into the bloodstream of a patient, as compared with thesystems that employ imperfect and fault-prone Gortex® or Teflon® airfilters. Furthermore, elimination of such filters eliminates the needfor EtO sterilization. Consequently, more efficient and convenient formsof sterilization, such as gamma sterilization and electron beamsterilization, can be used to sterilize certain embodiments of theadaptor 200. Manufacturers can thereby benefit from the resulting costsavings and productivity increases. In some embodiments, filters can beused at one or more points between the bag 260 and the regulatoraperture 250.

Advantageously, in certain embodiments, the bag 260 comprises an elasticmaterial. Accordingly, as the bag 260 expands within the vial 210, arestorative force arises within the bag 260 that tends to contract thebag 260. In some instances the restorative force is fairly small, andcan be balanced by a force within a syringe that is coupled to theadaptor 200. For example, the restorative force can be balanced byfriction between the plunger and the interior wall of the syringe.Consequently, in some instances, the restorative force does not affectthe withdrawal of an accurate amount of fluid from the vial 210.However, when the syringe is decoupled from the adaptor 200, therestorative force of the expanded bag 260 is no longer balanced. As aresult, the bag 260 tends to contract, which encourages fluid within theextractor channel 245 to return to the vial 210. Accordingly, theadaptor 200 can reduce the likelihood that fluid will spurt from thevial 210 when the syringe is decoupled therefrom, which is particularlybeneficial when oncology drugs are being removed from the vial 210. Whenthe adaptor 200 is used with the medical connector 241 (see FIG. 4),such as the Clave® connector, attached to the medical connectorinterface 240, the adaptor 200 can be substantially sealed in a rapidmanner after removal of the syringe from the proximal end of the medicalconnector 240.

In certain embodiments, a syringe or some other medical device can bedecoupled from the adaptor 200 after a portion of fluid has been removedfrom the vial 210 and then re-coupled with the adaptor 200, such as toreturn unwanted or excess liquid or air to the vial.

In some embodiments, multiple doses can be removed from the vial 210 viathe adaptor 200. For example, in some embodiments a first syringe iscoupled with the adaptor 200 and a first dose is removed from the vial210. The first syringe is then decoupled from the adaptor. Similarly, asecond syringe is then coupled with the adaptor 200 (or the firstsyringe is coupled with the adaptor 200 for a second time), a seconddose is removed from the vial 210, and the second syringe (or the firstsyringe) is decoupled from the adaptor 200. In like manner, numerousdoses can be removed from the same vial 210 via the adaptor 200.

In some embodiments, the vial 210 contains a powder, a concentratedliquid, or some other substance that is diluted prior to administrationthereof to a patient. Accordingly, in certain embodiments, a diluent isinfused into the vial 210 via the adaptor 200. In some embodiments, asyringe containing the diluent is coupled with the adaptor 200. The vial210 can be placed upright on a hard surface and the plunger of thesyringe can be depressed to urge the diluent through the adaptor 200 andinto the vial 210. The plunger can be released and allowed to back outof the syringe until pressure within the vial 210 is equalized. In someembodiments, the syringe is decoupled from the adaptor 200, the same ora different syringe or some other medical device is coupled the adaptor200, and the diluted contents of the vial 210 are removed.

In certain embodiments, decoupling and re-coupling of a syringe or othermedical device, removal of multiple doses from the vial 210 via a singleadaptor 200, and/or infusing a diluent into the vial 210 is facilitatedwhen the adaptor 200 comprises a medical connector 240, such as theClave® connector.

As noted above, in some instances the vial 210 is oriented with the cap214 pointing downward when liquid is removed from the vial 210. Incertain advantageous embodiments, the extractor aperture 246 is locatedadjacent a bottom surface of the cap 214, thereby allowing removal ofmost or substantially all of the liquid in the vial 210. In otherarrangements, the adaptor 200 comprises more than one extractor aperture246 to aid in the removal of substantially all of the liquid in the vial210. In some embodiments, the distal end 223 of the piercing member 220is spaced away from the extractor aperture 246. Such arrangementsadvantageously allow fluid to flow through the extractor aperture 246unobstructed as the distal portion 268 of the bag 260 expands.

FIG. 8 illustrates another embodiment of an adaptor 300. The adaptor 300resembles the adaptor 200 discussed above in many respects. Accordingly,numerals used to identify features of the adaptor 200 are incremented bya factor of 100 to identify like features of the adaptor 300. Thisnumbering convention generally applies to the remainder of the figures.

In certain embodiments, the adaptor 300 comprises a medical connectorinterface 340, a cap connector 330, a piercing member 320, and a bag360. The piercing member comprises a sheath 322 having a distal end 323.The piercing member 320 differs from the piercing member 220 in that itdoes not comprise a separate tip. Rather, the distal end 323 isconfigured to pierce the septum 216. In the illustrated embodiment, thedistal end 323 is angled from one side of the sheath 322 to another.Other configurations and structures are also possible. In manyembodiments, the distal end 323 provides a substantially unobstructedpath through which the bag 360 can be deployed. The distal end 323preferably comprises rounded or beveled edges to prevent the bag 360from ripping or tearing thereon. In some instances, the distal end 323is sufficiently sharp to pierce the septum 216 when the adaptor 300 iscoupled with the vial 210, but insufficiently sharp to pierce or damagethe bag 360 when the bag 360 is deployed or expanded within the vial210.

FIG. 9 illustrates another embodiment of an adaptor 301 that is similarto the adaptor 300 in some respects, but differs in others such as thosenoted hereafter. The adaptor 301 comprises a piercing member 380 thatsubstantially resembles the piercing member 320. In certain embodiments,however, the piercing member 380 is shorter than the piercing member320, and thus does not extend as far into the vial 210. Accordingly, thepiercing member 380 provides less of an obstruction to the bag 360 as itexpands to fill (or partially fill) the vial 210. In furtherembodiments, the piercing member 380 comprises a bag 360 having multiplefolds. The multiple folds allow the bag 360 to fit more compactly intothe smaller volume of the piercing member 380 than is available in thepiercing member 320.

In certain embodiments, the piercing member 380 comprises a flexibleshield 385 extending around the periphery of a tip 386 of the piercingmember 380. The shield can comprise, for example, plastic or rubber. Theshield 385 can be adhered to an inner wall of the piercing member 380,or it can be tensioned in place. In certain embodiments, at least aportion of the shield 385 is inverted (as shown) when in a relaxedstate. As the bag 360 is deployed, it forces a portion of the shield 385outward from the tip 386. In some embodiments, the shield 385 is sizedand dimensioned to extend to an outer surface of the tip 386 as the bag360 expands. The shield 385 thus constitutes a barrier between the tip386 and the bag 360 that protects the bag 360 from punctures, rips, ortears as the bag 360 expands.

In some arrangements, the adaptor 301 comprises a filter 390. In manyembodiments, the filter 390 is associated with the regulator channel325. The filter 390 can be located at the regulator aperture 350, withinthe regulator channel 325, or within the bag 360. For example, in someinstances, the filter 390 extends across the regulator aperture 350, andin other instances, the filter 390 extends across the bag aperture 364.In some arrangements, the filter 390 is a hydrophobic filter which couldprevent fluid from exiting the vial 210 in the unlikely event that thebag 360 ever ruptured during use. In such arrangements, air would beable to bypass the filter in proceeding into or out of the bag 360, butfluid passing through the ruptured bag 360 and through the regulatorchannel 325 would be stopped by the filter 390.

In the illustrated embodiment, the cap connector 330 of the adaptor 301comprises a skirt 336 configured to encircle a portion of the vial 210.In some embodiments, the skirt 336 can extend around less than theentire circumference of the vial 210. For example, the skirt 336 canhave a longitudinal slit. Advantageously, the skirt 336 can extenddistally beyond the tip 386 of the piercing member 380. Thisconfiguration partially shields the tip 386 from users prior toinsertion of the piercing member 380 into the vial 210, thereby helpingto prevent accidental contact with the tip 386. The skirt 336 furtherprovides a coupled adaptor 301 and vial 210 with a lower center of mass,thereby making the coupled items less likely to tip over.

FIG. 10 illustrates an embodiment of an adaptor 400 that resembles theadaptors 200, 300 described above in many ways, but comprises a piercingmember 420 that differs from the piercing members 220, 320 in mannerssuch as those now described. The piercing member 420 comprises a sheath422, a tip 424, and a piercing member aperture 402. In certainembodiments, the tip 424 is substantially conical and comes to a pointnear an axial center of the piercing member 420. In some embodiments,the tip 424 is permanently attached to the sheath 422, and can beintegrally formed therewith. The piercing member aperture 402 can belocated proximal to the tip 424. The piercing member aperture 402 canassume a wide variety of shapes and sizes. In some configurations, it isdesirable that a measurement of the piercing member aperture 402 in atleast one direction (e.g., the longitudinal direction) have ameasurement greater than the cross-sectional width of the piercingmember 420 to facilitate the insertion of a bag 460 (shown in FIG. 11)through the aperture 402 during assembly of the adaptor 400. In someinstances, the size and shape of the piercing member aperture 402 isoptimized to allow a large portion of the bag 460 to pass therethroughwhen the bag 460 is deployed within the vial 210, while not compromisingthe structural integrity of the piercing member 420.

FIG. 11 illustrates the adaptor 400 coupled with the vial 210. In theillustrated embodiment, the bag 460 is partially deployed within thevial 210. In certain embodiments, the bag 460 is configured to expandwithin the vial 210 and to fill a substantial portion thereof. As withthe bag 260, the bag 460 can comprise an expandable material or anon-expandable material. In certain embodiments, the bag 460 comprisesportions that are thicker near the piercing member aperture 402 in orderto prevent rips or tears. In some instances, the piercing memberaperture 402 comprises rounded or beveled edges for the same purpose.

As illustrated, in certain embodiments, the piercing member aperture 402is located on a side of the piercing member 420 opposite an extractoraperture 446. Such arrangements can allow fluid to pass through theextractor aperture 446 unobstructed as the bag 460 expands within thevial 210.

FIGS. 12A-12D illustrate two embodiments of an adaptor 500. The adaptor500 resembles the adaptors 200, 300 described above in many ways, butcomprises a piercing member 520 that differs in manners such as thosenow described. In certain embodiments, the piercing member 520 comprisestwo or more sleeve members 503 that house a bag 560 (shown in FIGS. 12Band 12D). In certain arrangements, the sleeve members 503 meet at aproximal base 504 of the piercing member 520. As described more fullybelow, in some configurations, the sleeve members 503 are integrallyformed from a unitary piece of material. In other configurations, thesleeve members 503 comprise separate pieces that are coupled with theproximal base 504.

In certain embodiments, such as the embodiment illustrated in FIGS. 12Aand 12B, the sleeve members 503 are biased toward an open configuration.In some instances, the bias is provided by the method used to create thesleeve members 503. For example, in some instances, two sleeve members503 and the proximal base 504 are integrally formed from a unitary pieceof pliable, molded plastic that substantially assumes a Y-shape, witheach sleeve member 503 comprising one branch of the “Y.” In otherinstances, the two sleeve members 503 comprise separate pieces that arecoupled with the proximal base 504. In certain of such instances, thesleeve members 503 are pivotally mounted to or bendable with respect tothe proximal base 504. The sleeve members 503 can be biased toward anopen configuration by a spring or by any other suitable biasing deviceor method. While configurations employing two sleeve members 503 havebeen described for the sake of convenience, the piercing member 520 cancomprise more than two sleeve members 503, and in variousconfigurations, comprises three, four, five, six, seven, or eight sleevemembers 503. In some instances, the number of sleeve members 503 ofwhich the piercing member 520 is comprised increases with increasingsize of the bag 560 and/or increasing size of the vial 210.

In some configurations, the bag 560 is inserted into the proximal base504. As described above with respect to the bag 260, the bag 560 may besecured within the proximal base 504 by some form of adhesive, by aplastic sheath, via tension provided by a relatively thick proximal endof the bag 560, or by any other suitable method.

In many embodiments, after insertion of the bag 560 into the proximalbase 504, the sleeve members 503 are brought together to form a tip 524.The tip 524 can assume any suitable shape for insertion through theseptum 216 (not shown) of the vial 210. In some arrangements, a jacket505 is provided around the sleeve members 503 to keep them in a closedconfiguration. The jacket 505 can be formed and then slid over the tip524, or it may be wrapped around the sleeve members 503 and securedthereafter. The jacket 505 preferably comprises a material sufficientlystrong to keep the sleeve members 503 in a closed configuration, yetcapable of easily sliding along an exterior surface thereof when thepiercing member 520 is inserted in the vial 210. In some instances, itis desirable that the material be capable of clinging to the septum 216.In various instances, the jacket 505 comprises heat shrink tubing,polyester, polyethylene, polypropylene, saran, latex rubber,polyisoprene, silicone rubber, or polyurethane. The jacket 505 can belocated anywhere along the length of the piercing member 520. In someembodiments, it can be advantageous to position the jacket 505 on thedistal portion of the sleeve members 503 to maintain the sleeve members503 close together to provide a sharp point for piercing the septum 216.

FIG. 12B illustrates an embodiment of the adaptor 500 having sleevemembers biased toward an open position coupled with the vial 210. Incertain embodiments, as the piercing member 520 is inserted into thevial 210, the jacket 505 catches on the septum 216 and remains on theexterior of the vial 210. As the piercing member 520 continues throughthe septum 216, the sleeve members 503 return to their naturally openstate, thus deploying the bag 560 within the vial 210. As fluid iswithdrawn from the vial 210, the bag 560 expands within the vial 210 ina manner such as that described above with respect to the bag 260.

In certain embodiments, such as the embodiment illustrated in FIGS. 12Cand 12D, the sleeve members 503 are biased toward a closedconfiguration. In some instances, the bias is provided by the methodused to create the sleeve members 503. For example, the sleeve members503 and the proximal base 504 can be integrally formed from a unitarypiece of molded plastic. During the molding process, or sometimethereafter, one or more slits 506 are formed in the molded plastic,thereby separating the sleeve members 503. In other instances the sleevemembers 503 comprise separate pieces that are attached to the proximalbase 504. In certain of such instances, the sleeve members 503 arepivotally mounted to the proximal base. The sleeve members 503 can bebiased toward a closed configuration by a spring or by any othersuitable biasing device.

In some configurations, the sleeve members 503 are opened to allow theinsertion of the bag 560 into the piercing member 520. The sleevemembers 503 return to their naturally closed state after insertion ofthe bag 560. As described above, the bag 560 can be secured within theproximal base 504 by any of numerous methods.

FIG. 12D illustrates an embodiment of the adaptor 500 having sleevemembers biased toward a closed position coupled with the vial 210. Incertain embodiments, the piercing member 520 is inserted into the vial210. As fluid is withdrawn from the vial 210, unbalanced pressurebetween the interior of the bag 560 and the interior of the vial 210causes the bag 560 to expand within the vial 210, thereby forcing openthe sleeve members 503. The bag 560 can continue to expand and furtherseparate the sleeve members 503.

FIG. 13 illustrates an embodiment of an adaptor 600 comprising aplurality of sleeve members 603. The adaptor 600 resembles the adaptors200, 300, 500 described above in many ways, but differs in manners suchas those now described. In certain embodiments, the adaptor 600comprises a medical connector interface 640, a cap connector 630, and apiercing member 620. In some embodiments, the piercing member 620comprises a projection 626, a bag connector 682, a sleeve 622, and a bag660. In some configurations, the interface 640, the cap connector 630,and the projection 626 are integrally formed of a unitary piece ofmaterial, such as polycarbonate plastic. In certain of suchconfigurations, the bag connector 682 is also integrally formedtherewith.

In certain embodiments, the bag connector 682 is attached to theprojection 626, preferably in substantially airtight engagement. In someembodiments, the bag connector 682 comprises a chamber 683 configured toaccept a distal extension 629 of the projection 626. In the illustratedembodiment, the bag connector 682 and chamber 683 define complimentarycylinders. A portion of the chamber 683, preferably a sidewall thereof,can be adhered to the distal extension 629 by glue, epoxy, or othersuitable means. A variety of other configurations for joining the bagconnector 682 and proximal portion 626 can be employed.

In some arrangements, the bag connector 682 is also attached to thesleeve 622. As illustrated in FIG. 14, in some arrangements, the sleeve622 comprises a proximal base 604 from which a plurality of sleevemembers 603 extend. In some instances, the proximal base 604 can definean opening 605. In various configurations, the sleeve 622 comprises two,three, four, five, six, seven, or eight sleeve members 603. More sleevemembers 603 are also possible. The sleeve members 603 can cooperate toform a cavity for housing the bag 660.

With reference again to FIG. 13, a portion of the bag connector 682 canbe inserted through the opening 605 of the proximal base 604. Theconnector 682 and proximal base 604 can be adhered to each other in someinstances, and can be secured to each other by a friction fit in others.Other methods of attachment are also possible. In many instances, theproximal base 604 remains fixed while the sleeve members 603 are allowedto move. The sleeve members 603 resemble the sleeve members 503described above, and can thus be biased toward an open configuration ora closed configuration. Accordingly, in some arrangements, a jacket (notshown) is used to retain sleeve members 603 that are biased toward anopen configuration in a closed configuration until the piercing member620 is inserted through the septum 216. In some instances, the jacket istrapped between the septum 216 and an interior surface of the capconnector 630, thereby helping to form a substantially airtight sealbetween the adaptor 600 and the vial 210.

In the illustrated embodiment, the bag connector 682 defines a portionof a regulator channel 625, which also extends through the projection626 of the piercing member 620, the cap connector 630, and a regulatoraperture 650. An extractor channel 645 extends from an extractoraperture 646 and through the proximal portion 626, the cap connector630, and the medical connector interface 640. In certain embodiments,the extractor aperture 646 is spaced away from the bag 660.

In some instances, the bag connector 682 comprises a nozzle 684 to whichthe bag 660 can be coupled. FIGS. 15A and 15B illustrate two embodimentsof the nozzle 684. In the embodiment illustrated in FIG. 15A, the nozzle684 is inserted into a proximal end 662 of the bag 660. The bag 660 canbe coupled to the nozzle 684 by any suitable means, such as by anadhesive, a plastic sleeve, a heat seal, or a tension fit. As describeabove with respect to the bag 360, in certain embodiments, asubstantially airtight tension fit is achieved when the proximal end 662of the bag 660 is sufficiently thick and stiff.

In the embodiment illustrated in FIG. 15B, the nozzle 684 comprises oneor more clip extensions 685. In some embodiments, a single clipextension 685 encircles the nozzle 684. Each of the one or more clipextensions 685 comprises a detent 686 and defines a recess 687. Incertain embodiments, a collar 688 is placed around the proximal end 662of the bag 660. The collar 688 is preferably sized and configured to fitsnugly within the recess 687 and to be held securely in place by thedetent 686 of each clip extension 685. Consequently, the one or moreclip extensions 685 in cooperation with the collar 688 form asubstantially airtight seal between the proximal end 662 of the bag 660and the nozzle 684.

With reference again to FIG. 15A, in certain embodiments, the bag 660 issubstantially cylindrical. In some embodiments, the walls of the bag 660are thicker than the base thereof. In certain embodiments, the walls ofthe bag 660 are between about 0.001 inches and 0.004 inches, betweenabout 0.001 inches and about 0.002 inches, between about 0.002 inchesand about 0.003 inches, or between about 0.003 inches and about 0.004inches thick. In other arrangements, the walls are greater than 0.001inches, greater than 0.002 inches, or greater than 0.003 inches thick.In still other arrangements, the walls are less than about 0.004 inches,less than about 0.003 inches, or less than about 0.002 inches thick.Cylindrical configurations can be advantageous for use with the vial 210when a large portion the vial 210 is generally cylindrical, as is oftenthe case with standard medicinal vials. The cylindrical bag 660 canexpand to a shape that substantially conforms to the interior volume ofthe vial 210.

As illustrated in FIG. 16, in some instances, the bag 660 can be foldedin a star-like configuration having multiple arms 661. Each arm 661 canbe folded, rolled, crumpled, or otherwise manipulated to fit within thepiercing member 620 when it is closed. Any number of arms 661 can beformed from the bag 660, and in certain instances, the number of arms661 increases with increasingly larger bags 660. In otherconfigurations, the bag 660 is molded or shaped such that it naturallyhas a star-shaped cross-section and is capable of expanding to fillsubstantially cylindrical vials 210. Other configurations of the bag 660are also possible, as discussed above in connection with the bag 260,and similar folding patterns may be employed.

FIG. 17 illustrates an embodiment of an adaptor 601 that resembles theadaptor 600 in many ways, but differs in manners such as those nowdescribed. The adaptor 601 comprises the piercing member 620 thatpartially defines the regulator channel 625, and further comprises asecondary piercing member 690 that partially defines the extractorchannel 645. Accordingly, the adaptor 601 punctures the septum 216 intwo distinct locations when coupled with the vial 210.

The secondary piercing member 690 can comprise any suitable material forpuncturing the septum 216. In various embodiments, the secondarypiercing member 690 comprises metal or plastic. In many configurations,the secondary piercing member 690 is significantly smaller than thepiercing member 620, which allows both piercing members 620, 690 to bereadily inserted through the septum 216. Furthermore, a smallersecondary piercing member 690 can position the extractor aperture 646,which is located at the tip of the secondary piercing member 690 in someconfigurations, adjacent an interior surface of the septum 216 when theadaptor 601 is coupled to the vial 210. Accordingly, most of the liquidcontents of the vial 210 may be removed when the vial 210 is turnedupside-down.

FIG. 18 illustrates an embodiment of an adaptor 602 that resembles theadaptor 600 in many ways, but differs in manners such as those nowdescribed. In the illustrated embodiment, the extractor channel 645extends through the proximal portion 626 of the piercing member 620 suchthat the extractor aperture 646 is located within, or at a positioninterior to an outer surface of, the sleeve 622. More generally, theextractor aperture 646 is located within, or at a position interior toan outer surface of, the piercing member 620. In certain embodiments, asshown, the bag connector 682 is configured to space the bag 660 awayfrom the extractor aperture 646 so that fluid may flow through theaperture 646 unobstructed as the bag 660 expands.

In certain embodiments, a ridge 694 extends around an inner surface ofthe cap connector 630 and defines a space 695 for accepting a jacket(not shown) used to keep the sleeve members 603 in a closedconfiguration. The space 695 can be of particular utility when thejacket has a substantial length or otherwise comprises a large amount ofmaterial.

FIG. 19 illustrates an embodiment of a vial adaptor 700. In certainembodiments, the adaptor 700 comprises a housing member 706, a sheath707, and a bag insertion member 708. In some embodiments, the housingmember 706 comprises a piercing member 720, a cap connector 730, and amedical connector interface 740 that in some ways resemble similarlynumbered features of various other adaptor embodiments described herein.

In certain embodiments, the medical connector interface 740 branchesfrom a proximal extension 709 of the housing member 706. The medicalconnector interface 740 defines a branch of a substantially “y”-shapedextractor channel 745. The piercing member 720 and the proximalextension 709 define the remainder of the extractor channel 745.

In certain embodiments, the cap connector 730 comprises one or moreprojections 737 for securing the adaptor 700 to the cap 214 of the vial210 (not shown). In some embodiments, the cap connector 730 comprisesone or more slits 739 that facilitate the coupling of the adaptor 700 tothe vial 210 by allowing the cap connector 730 to expand. In someconfigurations, the cap connector 730 comprises a skirt 736.

The piercing member 720 can resemble the piercing members describedherein. In some embodiments, the piercing member 720 comprises an angleddistal end 723 which allows the passage therethrough of the baginsertion member 708. Advantageously, in some embodiments, the piercingmember 720 is configured to extend only a short distance into the vial210. Accordingly, a large amount of fluid can be withdrawn from the vial210 when the vial 210 is oriented with the cap 214 facing downward. Bybeing shorter, the piercing member 720 can also have thinner wallswithout the risk of bending or breaking upon insertion into the vial210. Thinner walls can allow the insertion of a larger bag 760 thanwould otherwise be possible, thus permitting the safe and accuratewithdrawal of a larger amount of fluid from the vial 210 in someinstances. In some embodiments, the piercing member 720 does not extendbeyond the skirt 736, which helps to shield users from accidentalcontact with the piercing member 720.

In some embodiments, the proximal extension 709 of the housing member706 is coupled with the sheath 707. In certain instances, the proximalextension 709 and the housing member 706 are joined in threaded,snapped, or friction-fit engagement. In some instances, the proximalextension 709 and the housing member 706 are joined by glue, epoxy,ultrasonic welding, etc. In further arrangements, the proximal extension709 and the housing member 706 are integrally formed of a unitary pieceof material. In some arrangements, the proximal extension 709 and thehousing member 706 are coupled in substantially airtight engagement.

In some embodiments, the proximal extension 709 and the sheath 707 areconfigured to secure a sealing member 715 in place. In someconfigurations, the proximal extension 709 comprises a shelf 717 thatextends around an inner perimeter thereof, and the sheath 707 comprisesridge 719 that extends around an inner perimeter thereof. The shelf 717and the ridge 719 can be configured to tension the sealing member 715 inplace. In some arrangements, the sealing member 715 is slightlycompressed by the shelf 717 and the ridge 719. In further arrangements,the sealing member 715 is held in place by glue or some other adhesive.In other embodiments, the sealing member 715 is retained in a groove inthe bag insertion member 708.

The sealing member 715 can comprise any suitable material for forming asubstantially airtight seal with the bag insertion member 708 whilebeing slidably engaged therewith. In some instances, the sealing member715 comprises a standard O-ring as is known in the art. In otherinstances, the sealing member 715 comprises a flange or otherconfiguration that permits movement of the bag insertion member 708 inone direction only, such as to be inserted in the vial 210. In someinstances, the substantially airtight seal between the sealing member715 and the bag insertion member 708 defines a proximal boundary of theextractor channel 745.

In certain embodiments, the sheath 707 is sized and dimensioned to begripped by a user—in various instances, with one, two, three, or fourfingers of one hand of the user. The sheath 707 can be substantiallyhollow, defining a chamber 751 through which the bag insertion member708 can move. In some embodiments, the chamber 751 narrows toward thedistal end thereof. The sheath 707 can also define a slot 752. In someinstances, the slot 752 has a substantially constant width, while inothers, the slot 752 narrows toward a distal end thereof. The slot 752can comprise a locking mechanism, as described below.

In various arrangements, a tab 753 is attached to or integrally formedwith the bag insertion member 708. The tab 753 can be sized anddimensioned to be easily manipulated by a user—in some instances, by athumb of the user. The tab 753 can be rounded to prevent any snagsthereon by gloves that might be worn by the user. The tab 753 isgenerally configured to cooperate with the slot 752. In somearrangements, the tab 753 extends radially outward from the proximal endof the bag insertion member 753 and through the slot 752. The tab 753and the slot 752 can be sized and configured such that the tab 753 canslide along a length of the slot 752. In some arrangements, the distalend of the slot 752 is sized such that the tab 753 fits snugly therein.

FIGS. 20A and 20B illustrate two separate locking mechanisms that can beused to secure the tab 753 at some fixed position in the slot 752. FIG.20A illustrates a clip 754. The clip 754 comprises an angled face 755and a ridge 756, and is biased toward a closed position, as illustrated.As the tab 753 is advanced toward the distal end of the slot 752, itcontacts the face 755 and forces the clip 754 toward an open position.Once the tab 753 has been advanced to the distal end of the slot 752,the clip 754 is free to return to its natural, closed position.Accordingly, the ridge 756 contacts a proximal surface of the tab 753and holds the tab 753 in place. As shown, in some arrangements, theridge 756 is curved such that the clip 754 will not spring back intoplace until the tab 753 has reached the distal end of the slot 752, andonce the clip 754 does spring back into place, a portion of the ridge756 remains in contact with the clip 754. In other arrangements, morethan one clip 754 can be used. For example, one clip 754 can be locatedon each side of the slot 752 to provide greater stability to the tab 753when locked in place. In other instances, the one or more clips 754comprise ridges extending from the sides of the slot 752 and areintegrally formed with the sheath 707. In such instances, the clips 754can be substantially smaller than those shown, and need not moveindependently from the sheath 707.

FIG. 20B illustrates an alternative arrangement of the slot 752 that canprovide a locking mechanism for the tab 753. In the illustratedembodiment, the slot 752 comprises a lateral extension 757 that has aheight corresponding to the height of the tab 753. Accordingly, once thetab 753 is advanced to the distal end of the slot 752, the tab 753 canbe rotated into the lateral extension 757. In some instances, the tab753 is secured in the lateral extension 757 by a friction fit. In otherinstances, a clip 754 can be used. Any other suitable means for lockingthe tab 753 in place can be employed.

With reference again to FIG. 19, in certain embodiments, the baginsertion member 708 comprises a flange 754 configured to help securelylock the tab 753 in place. The flange 754 can be attached to orintegrally formed with the bag insertion member 708, and in certaininstances, comprises a unitary piece with the tab 753. As noted above,in certain arrangements, the chamber 751 narrows toward the distal endof the sheath 707. Accordingly, as the bag insertion member 708 isadvanced toward the distal end of the sheath 707, the flange 754contacts a sidewall of the chamber 751, thereby restricting movement ofthe proximal end of the bag insertion member 708.

In certain embodiments, the bag insertion member 708 comprises a hollowshaft 753. In some arrangements, the shaft 753 extends from a proximalend of the sheath 707 to the distal end 723 of the piercing member 720.The shaft 753 can define a regulator channel 725 through which ambientair may flow.

In some arrangements, the bag insertion member 708 comprises thinnerwalls at its distal end to allow room for the bag 760 within theextractor channel 745. The bag 760 can be attached to the bag insertionmember 708 by any suitable means, such as those described above withrespect to the bag 260. In some arrangements, only the distal end 762 ofthe bag 760 is attached to the bag insertion member 708, thus freeingthe remainder of the bag 760 to expand within the vial 210. In someinstances, the bag 760 is substantially cylindrical in order to conformto the volume of the vial 210. The bag 760 can be configured to expandboth laterally and longitudinally.

In certain arrangements, the bag insertion member 708 is configured toadvance the bag 760 to a distance within the vial 210 sufficient toensure that the bag 760 does not obstruct fluid flow through the distalend 723 of the piercing member 720. As indicated above, in someembodiments, the bag insertion member 708 is locked in place once it isadvanced into the vial 210. Because the bag insertion member 708generally cannot thereafter be withdrawn from the vial 210, there is areduced chance of puncturing or tearing the bag 760 on the distal tip723 after the bag 760 has expanded laterally.

Certain processes for using the adaptor 700 resemble those describedabove with respect to the adaptor 200 in many ways, and can includeadditional or alternative procedures such as those now described. Incertain instances, once the adaptor 700 is coupled with the vial 210,the tab 753 is advanced distally along the slot 752, thus advancing thebag 760 toward the interior of the vial 210. In some instances, the tab753 is locked in place at the distal end of the slot 752. In someinstances, a user grips the sheath 707 with one or more fingers of onehand and advances the tab 753 distally within the slot 752 with thethumb of the hand until the tab 753 locks in place. Other grippingarrangements can also be employed.

In some instances, fluid is withdrawn from the vial 210 through thedistal end 723 and through the extractor channel 745, and the bag 760consequently expands with air. The air can flow through a regulatoraperture 750, through the regulator channel 725 and into the bag 760. Inother instances, fluid is injected into the vial 210 via the extractorchannel 745 and the distal end 723, and air is forced from the bag 760.The expelled air can follow the reverse path through the regulatorchannel 725.

FIG. 21 illustrates an embodiment of an adaptor 800 in a disassembledstate. The adaptor 800 comprises a housing member 806, a bag 860, and acasing member 870. In certain embodiments, the adaptor 800 is configuredto provide sterilized air to the vial 210 as fluid is withdrawntherefrom.

With reference to FIGS. 21, 22, and 23, in certain embodiments, thehousing member 806 comprises a cap connector 830, a piercing member 820,and a proximal extension 809 which, in some arrangements, are integrallyformed of a unitary piece of material. In some embodiments, the housingmember comprises polycarbonate plastic.

The cap connector 830 resembles similarly numbered cap connectorsdescribed above in many ways. In some instances, the cap connector 830comprises one or more projections 837 and/or one or more slits 839. Insome arrangements, an inner ring 835 and an outer ring 836 project froma proximal surface of the cap connector 830. The inner ring 835 can beconfigured to couple with the bag 860, as described below. The outerring 836 can be configured to couple with the casing member 870,preferably in substantially airtight engagement via any suitable means,including those described herein.

In certain arrangements, the piercing member 820 extends distally from acentral portion of the cap connector 830 and the proximal extension 809extends proximally from the central portion of the cap connector 830.Together, the piercing member 820 and proximal extension 809 define anouter boundary of both a regulator channel 825 and an extractor channel845. An inner wall 827 defines an inner boundary between the regulatorchannel 825 and the extractor channel 845.

In some arrangements, the piercing member 820 defines a distal regulatoraperture 850 a configured to be located within the vial 210 when theadaptor 800 is coupled therewith. The distal regulator aperture 850 apermits fluid communication between the vial 210 and the regulatorchannel 825. The piercing member 820 can also define a distal extractoraperture 846 a. Advantageously, the distal extractor aperture 846 a canbe configured to be located adjacent an interior surface of the septum216 when the adaptor 800 is coupled with the vial 210, therebypermitting withdrawal of most or all of the liquid from the vial 210through the extractor channel 845.

In certain configurations, the proximal extension 809 defines a proximalregulator aperture 850 b that allows fluid communication between the bag860 and the regulator channel 825. The proximal regulator aperture 850 bcan be located anywhere along the length of the portion of the proximalextension 809 that defines the outer boundary of the regulator channel825, and can assume various sizes. In some instances, the proximalregulator aperture 805 b is located at or adjacent the longitudinalcenter of the proximal extension 809. In certain configurations, thepurpose of the above-noted portion of the proximal extension 809 isprimarily structural. Accordingly, in some arrangements, this portion iseliminated, and the proximal regulator aperture 850 b is instead definedby the cap connector 830. The proximal extension 809 can also define aproximal extractor aperture 846 b that allows fluid communicationbetween a medical connector interface 840 and the extractor channel 845.

With reference to FIGS. 21 and 23, in certain embodiments, the casingmember 870 defines a cavity 871 for housing the bag 860. The casingmember 870 can comprise the medical connector interface 840, whichresembles similarly numbered medical connector interfaces describedabove in many ways. In certain arrangements, a base portion of themedical connector interface 840 is configured to accept a proximal end872 of the proximal extension 809. In some arrangements, the proximalend 872 is attached to the casing member 870 in substantially airtightengagement via any suitable means, including those disclosed herein. Insome arrangements, the casing member 870 comprises a venting aperture873. The venting aperture 873 allows ambient air to enter the chamber871, thereby exposing an exterior surface of the bag 860 to atmosphericpressure, described in more detail below. The casing member 870 cancomprise a proximal ring 874 for coupling the casing member 870 with thebag 860, as discussed below. The casing member 870 preferably comprisesa rigid material capable of protecting the bag 860, and in someinstances comprises polycarbonate plastic.

In some arrangements, the bag 860 comprises a proximal flange 861 and adistal flange 862. The proximal flange 861 can be sized and configuredto couple with the proximal ring 874 of the casing member 870, and thedistal flange 862 can be sized and configured to couple with the innerring 835 of the housing member 806, preferably in substantially airtightengagement. In some instances, a substantially airtight engagement isachieved with flanges 861, 862 that comprise stiffer and/or thickermaterial than the remainder of the bag 860. In further arrangements, aninner diameter of the flanges 861, 862 is slightly smaller than an outerdiameter of the rings 874, 835, respectively. In some arrangements, theflanges 861, 862 are adhered to the rings 874, 835, respectively.

In various configurations, the inner diameter of either of the flanges861, 862 is from about 0.10 to about 0.40 inches, from about 0.15 toabout 0.35, or from about 0.20 to about 0.30 inches. In otherconfigurations, the inner diameter is at least about 0.10 inches, atleast about 0.15 inches, at least about 0.20 inches, or at least about0.25 inches. In still other configurations, the inner diameter is nomore than about 0.30 inches, no more than about 0.35 inches, or no morethan about 0.40 inches. In some embodiments, the inner diameter is about0.25 inches.

In various configurations, the height of the bag 860, as measured fromtip to tip of the flanges 861, 862, is from about 1.00 to 3.00 inches,from about 1.50 to 2.50 inches, or from about 1.75 to about 2.25 inches.In other configurations, the height is at least about 1.00 inches, atleast about 1.50 inches, at least about 1.75 inches, or at least about2.00 inches. In still other configurations, the height is no more thanabout 2.25 inches, no more than about 2.50 inches, or no more than about3.00 inches. In some embodiments, the height is about 2.00 inches.

In various configurations, the width of the bag 860 is from about 0.80inches to about 1.00 inches, from about 0.85 inches to about 0.95inches, or from about 0.87 to about 0.89 inches. In otherconfigurations, the width is at least about 0.80 inches, at least about0.85 inches, or at least about 0.87 inches. In still otherconfigurations, the width is no more than about 0.89 inches, no morethan about 0.95 inches, or no more than about 1.00 inches. In someconfigurations, the width is about 0.875 inches. In some configurations,the thickness of the bag 860 is from about 0.0005 inches to about 0.010inches. In many arrangements, the bag 860 is sufficiently thick toresist tearing or puncturing during manufacture or use, but sufficientlyflexible to contract under relatively small pressure differentials, suchas pressure differentials no more than about 1 psi, no more than about 2psi, no more than about 3 psi, no more than about 4 psi, or no more thanabout 5 psi.

In some embodiments, the bag 860 is both circularly symmetric andsymmetric about a latitudinal plane passing through a center of the bag860. In such embodiments, assembly of the adaptor 800 is facilitatedbecause the bag 860 can assume any of a number of equally acceptableorientations within the adaptor 800.

In certain arrangements, the bag 860 comprises sterilized air that canbe drawn into the vial 210 (not shown) as fluid is withdrawn therefrom.In some arrangements, the air within the bag 860 is pressurized tocorrespond with the approximate atmospheric pressure at which theadaptor 800 is expected to be used. In some instances, a removable coveror tab 875 (shown in FIG. 22) is placed over the distal regulatoraperture 850 a in order to maintain the pressure within the bag 860 andto ensure that the air within the bag 860 remains sterile up throughcoupling of the adaptor 800 with the vial 210. As with the jacket 505described above, the tab 875 can be configured to catch on the septum216 and remain there as the piercing member 820 is inserted through theseptum 216. Other suitable methods can also be used for maintaining thepressure within the bag 860 and ensuring that the air within the bag 860remains sterile up through coupling of the adaptor 800 with the vial210.

In some instances, when the adaptor 800 is coupled with the vial 210,the atmospheric pressure within the extractor channel 845 correspondswith the pressure within the bag 860. As fluid is withdrawn from thevial 210, the pressure within the vial 210 drops. Accordingly,sterilized air flows from the bag 860 into the vial 210. For reasonsdiscussed above in connection with other adaptors, in some embodiments,the bag 860 comprises a volume of air equal to or greater than thevolume of fluid contained in the vial 210. In some arrangements, the bag860 is also preferably configured to readily collapse.

In certain configurations, as fluid is withdrawn from the vial 210, itflows through the distal extractor aperture 846 a, the extractor channel845, the proximal extractor aperture 846 b, and the medical connectorinterface 840. As pressure drops within the vial 210, sterilized air iswithdrawn from the bag 860, through the proximal regulator aperture 850b, through the regulator channel 825, through the distal regulatoraperture 850 a, and into the vial 210.

In some instances, excess fluid and/or bubbles are returned to the vial210. Injecting fluid and/or air into the vial 210 increases pressurewithin the vial 210. As a result, in some arrangements, air and/or fluidwithin the vial 210 flows through the distal regulator aperture 850 ainto the regulator channel 825. In some instances, the air and/or fluidadditionally flows into the bag 860. In many instances, it is desirableto prevent fluid from flowing into the bag 860. Accordingly, in somearrangements, the proximal regulator aperture 850 b can be small so aspermit air to flow therethrough but resist introduction of fluid to thebag 860. In other arrangements, a hydrophobic filter, membrane, or meshis disposed over the proximal regulator aperture 850 b. The adaptor 800thus can be particularly suited to allow the expulsion of excess fluidor air bubbles from a syringe or other medical instrument.

FIG. 24 illustrates an embodiment of a vial adaptor 900 coupled with thevial 210. The adaptor 900 comprises a medical connector interface 940, acap connector 930, and a piercing member 920. The adaptor 900 furthercomprises an input port 980 and regulator port 981. In certainembodiments, the ports 980, 981 are disposed at opposite ends of theadaptor 900 in order to balance the adaptor 900. As shown, in someembodiments, a single housing comprises each of the above-notedfeatures. The housing can comprise any rigid material, such as plastic.

In some embodiments, the medical connector interface 940 and the capconnector interface 930 represent similarly numbered features describedabove. In the illustrated embodiment, the cap connector 930 comprises aplatform 939.

In certain embodiments, the piercing member 920 defines an extractoraperture 946, a distal portion of an extractor channel 945, a regulatoraperture 950, and a distal portion of a regulator channel 925. Theapertures 946, 950 can be positioned on the sides of the piercing member920 or at a distal end 923 thereof, as illustrated.

In certain embodiments, the extractor channel 945 extends through thepiercing member 920, through the cap connector 930, and through themedical connector interface 940. The regulator channel 925 extendsthrough the piercing member 920, through the cap connector 930, and intothe ports 980, 981.

In some embodiments, the input port 980 comprises a hydrophobic filter990. Such filters are generally known in the art. The filter 990prevents dust, bacteria, microbes, spores, and other contaminants fromentering the vial 210. In some embodiments, the input port 980 comprisesa valve 984. The valve 984 is configured to permit air that has passedthrough the filter 990 to pass into the regulator channel 925, but toprevent any air or fluid from passing through the valve 984 in the otherdirection.

In some embodiments, the regulator port 981 comprises a hydrophobicfilter 991. In some instances, the filter 991 is identical to the filter990. However, in many embodiments, the hydrophobic filter need only becapable of prohibiting the passage therethrough of liquids or vapors,whether or not it is capable of filtering out dust, bacteria, etc. Inmany embodiments, the regulator port 981 comprises a bag 960 insubstantially airtight engagement with the port 981. In some instances,the bag 960 comprises a flexible material capable of expanding andcontracting. In many instances, the bag 960 comprises a substantiallyimpervious material. In certain configurations, the bag 960 comprisesMylar®, polyester, polyethylene, polypropylene, saran, latex rubber,polyisoprene, silicone rubber, and polyurethane.

In some configurations, as fluid is withdrawn from the vial 210 throughthe extractor channel 945, ambient air passes through the filter 990,through the valve 984, through the regulator channel 925, and into thevial 210. The bag 960, if not already inflated, tends to inflate withinthe regulator port 981 due to pressure within the vial 210 being lowerthan atmospheric pressure.

In certain configurations, as fluid and/or air is returned to the vial210, pressure within the vial 210 increases. Fluid is thus forced intothe regulator channel 925. Because the valve 984 prevents passagetherethrough of fluid, the fluid fills the regulator channel 925 andcollapses the bag 960. So long as the volume of fluid returned to thevial 210 is smaller than the volume of the bag 960, the pressure withinthe vial 210 generally does not increase significantly. However, oncethe bag 960 is completely collapsed, additional return of fluid to thevial 210 generally increases the pressure within the vial 210.Accordingly, in some arrangements, the size of the bag 960 determinesthe amount of overdrawn fluid that can be returned to the vial 210without causing any of the pressure-related problems described above. Invarious embodiments, the bag 960, when expanded, has a volume of betweenabout 0.5 cc and 5 cc, between about 1 cc and 4 cc, or between about 1.5cc and about 2 cc. In some embodiments the volume is no more than about2 cc or no more than about 1 cc. In some instances, the adaptor 900houses a relatively small bag 960 having a volume of about 1 cc or about2 cc, for example, which permits the return of bubbles or small amountsof overdrawn fluid while keeping the adaptor 900 from being overlybulky.

In certain embodiments, the presence of filters 990, 991 that arehydrophobic can be precautionary and may not be warranted. In principle,the valve 984 and the substantially impervious bag 960 should preventany fluid from passing from the vial 210 to the exterior of the adaptor900. However, in the unlikely event that the valve 984 were to fail orthe bag 960 were to rupture, the hydrophobic filters 990, 991 couldserve to prevent fluid from exiting the adaptor 900. Similarly, in someinstances, the collapsible bag 960 is removed from the regulator port991 and/or the valve 984 is removed from the input port 980 withoutaffecting the operation of the adaptor 900.

FIG. 25 illustrates an embodiment of an adaptor 1000 coupled with a vial1210. The adaptor 1000 comprises a medical device interface 1040, a capconnector 1030, and a piercing member 1020, each of which resemblessimilarly numbered features described herein in many ways. In someembodiments, the adaptor 1000 comprises an extractor channel 1045 forremoving fluid from the vial 1210, but does not comprise a regulatorchannel. The vial 1210 resembles the vial 210 except as detailedhereafter.

In certain embodiments, the vial 1210 comprises a regulator conduit 1215coupled at one end with a bag 1260, preferably in substantially airtightengagement. In some embodiments, the regulator conduit 1215 extendsthrough the septum 216 and through the casing 218. In such embodiments,the portion of the septum 216 that is normally visible to a user issubstantially unaffected by the presence of the conduit 1215, asillustrated in FIG. 26. Accordingly, a user would generally not riskaccidentally trying to insert the piercing member 1020 into or over theregulator conduit 1215. In other embodiments, the regulator conduit 1215extends through the septum 216 only. In still other embodiments, theregulator conduit 1215 extends through the body 212 of the vial 1210. Insome embodiments, especially those in which a syringe with a needle isexpected to pierce the vial 1210, the regulator conduit 1215 can besubstantially longer than is shown in the illustrated embodiment toavoid puncture of the bag 1260 by the needle. In some instances, theregulator conduit 1215 can extend further into the vial 1210 than themaximum distance that a needle can extend into the vial 1210. Theregulator conduit 1215 can extend at least about ¼, ⅓, ½, ¾, orsubstantially all of the distance from the interior wall of the vial1210. The regulator conduit 1215 can also be curved to conform with thecurved shape of the neck portion of a standard vial. In this way, theregulator conduit 1215 can help to position the bag 1260 as far aspossible from a needle or piercing member 1020 that penetrates theseptum 216. In certain instances, the vial 1210 is filled with a medicalfluid, is slightly evacuated, and is then hermetically sealed. In manyembodiments, the bag 1260 is included in the sealed vial 1210 in agenerally collapsed state. However, atmospheric pressure acting on theinterior of the bag 1260 can cause it to expand slightly within thesealed vial 1210 in some instances.

The adaptor 1000 can be coupled to the vial 1210. In some instances,insertion of the piercing member 1020 results in slight pressure changeswithin the vial 1210 that force the bag 1260 away from the piercingmember 1020. In certain arrangements, the piercing member 1020 extendsjust beyond a distal surface of the septum 216, and is spaced away fromthe bag 260. It is appreciated that any adaptor disclosed herein couldbe coupled with the vial 1210, as could numerous other adaptorsconfigured to be coupled with a standard medicinal vial. As fluid iswithdrawn from the vial 1210 or injected into the vial 1210, the bag1260 expands and contracts, respectively, in a manner as disclosedherein.

In certain embodiments, the vial 1210 comprises one or more extensions1230. The extensions 1230 can be disposed around the perimeter of thecap 214, as shown, or they can be located at other points on the cap214. In some instances, the one or more extensions 1230 are located on adistal side of the cap 214, on a proximal side of the cap 214, and/oraround a surface extending between the proximal and distal sides of thecap 214. In many arrangements, the extensions 1230 extend only a shortdistance around the perimeter of the cap 214. In many arrangements, theextensions 1230 maintain space between the cap 214 and the cap connector1030 when the vial adaptor 1000 is coupled with the vial 1210, thusallowing ambient air to flow freely into and/or out of the regulatorconduit 1215. In other embodiments, the vial adaptor 1000 comprisesextensions 1230 for the same purpose. Other arrangements are possiblefor permitting air to flow freely into and/or out of the regulatorconduit 1215. For example, the vial adaptor 1000 can comprise a ventingchannel (not shown) extending through the cap connector 1230.

FIG. 27 illustrates an embodiment of a vial 1310 comprising a bag 1360coupled with the adaptor 1000. In some embodiments, the bag 1360 isfilled with a medical fluid 1320. A distal end 1362 of the bag 1360 canbe hermetically sealed to the cap 214. In some instances, the distal end1362 is sealed between the septum 216 and a proximal end of the body212. In certain embodiments, the vial 1310 comprises a venting aperture1325. The venting aperture 1325 can be located anywhere on the body 212.In some arrangements, the venting aperture 1325 is located at a distalend of the body 212. Accordingly, the bag 1360 does not obstruct theventing aperture 1325 when fluid is withdrawn from the vial 1310 in anupside-down configuration. In some instances, the venting aperture 1325is covered by a filter or a screen to prevent debris or other items fromentering the vial 1310 and possibly puncturing the bag 1360.

In certain instances, as a volume of fluid is withdrawn from the vial1310, the bag 1360 contracts to a new smaller volume to account for theamount of fluid withdrawn. In some instances, due to the ventingaperture 1325, the pressure surrounding the bag 1360 and the pressureacting on a device used to extract the fluid, such as a syringe, are thesame when fluid ceases to be withdrawn from the vial 1310. Accordingly,extraction of fluid from the vial 1310 can be similar to other methodsand systems described herein in many ways.

FIG. 28 illustrates an embodiment of a vial 1410 comprising a bag 1460.In some arrangements, the vial 1410 comprises a regulator conduit 1415coupled at one end with the bag 1460, preferably in substantiallyairtight engagement. In certain configurations, the regulator conduit1415 comprises a center wall 1417 and an outer wall 1419. In somearrangements, the center wall 1417 bisects the septum 216, extendingalong the diameter of the septum 216. The center wall 1417 can comprisea flange 1420 that extends proximally from the septum 216 along aportion thereof not covered by the casing 218. In some arrangements, theouter wall 1419 is sealed in substantially airtight engagement betweenthe septum 216 and a proximal end of the body 212. In someconfigurations, the outer wall 1419 is substantially semicircular.

Accordingly, in some embodiments, the septum 216 is divided into twoportions by the regulator conduit 1415. Piercing one portion of theseptum 216 provides access to the contents of the vial 1410, andpiercing the other portion of the septum 216 provides access to theregulator conduit 1415 and the bag 1460. In some configurations, atleast a proximal surface of the septum 216 is colored, painted, orotherwise marked to indicate the different portions of the septum 216.

FIG. 29 illustrates an embodiment of an adaptor 1500 coupled with thevial 1410. The adaptor 1500 comprises a medical connector interface 1540and a cap connector 1530 that resemble similarly numbered featuresdescribed herein. The cap connector 1530 can define a groove 1531 havingsufficient depth to accept the flange 1420 or to avoid contacttherewith.

In some configurations, the adaptor 1500 comprises an extractor piercingmember 1521 and a regulator piercing member 1522. In some embodiments,the extractor piercing member 1521 is configured to extend just beyond adistal surface of the septum 216. Accordingly, in some instances, theregulator piercing member 1522 is longer than the extractor piercingmember 1521, which provides a means for distinguishing the piercingmembers 1521, 1522 from each other. Other methods for distinguishing thepiercing members 1521, 1522 can also be employed. The adaptor 1500 canbe colored, painted, or otherwise marked to indicate correspondance withthe different sections of the septum 216.

In some instances, the extractor piercing member 1521 provides fluidcommunication with the liquid contents of the vial 1410, and theregulator piercing member 1522 provides fluid communication with the bag1460. Accordingly, removal of liquid from the vial 1410 via the adaptor1500 can be similar to other liquid removal methods and systemsdescribed herein in many ways.

FIG. 30 illustrates an embodiment of an adaptor 1600 in a disassembledstate. The adaptor 1600 can be coupled with a vial, such as the vial 210described above. The adaptor 1600 resembles the adaptors described abovein many ways, but differs in manners such as those discussed hereafter.Any suitable combination of features, structures, or characteristicsdescribed with respect to the adaptor 1600 and/or any other adaptordescribed herein is possible. In certain embodiments, the adaptor 1600comprises a plug 1601, a bag 1660, a channel housing member 1670, a tip1624, a sleeve 1680, a cap connector 1630, and a shroud 1690. In otherembodiments, the adaptor 1600 comprises fewer than all of these featuresor structures. For example, in some embodiments, the adaptor 1600 doesnot comprise the plug 1601, the sleeve 1680, and/or the shroud 1690. Insome arrangements, the channel housing member 1670 and the cap connector1630 comprise separate pieces, as shown. In other arrangements, thechannel housing member 1670 and the cap connector 1630 are integrallyformed of a unitary piece of material.

In certain embodiments, the adaptor 1600 comprises a piercing member1620. In some embodiments, the piercing member 1620 comprises the tip1624 and the sheath 1622, while in other embodiments, the piercingmember 1620 does not comprise the tip 1624. In certain arrangements, thetip 1624 is separable from the sheath 1622. In some instances, the tip1624 is secured to the sheath 1622 by a sleeve 1680. The sleeve 1680 canbe configured to cling to the septum 216 as the sheath 1622 is insertedthrough the septum 216, thereby remaining on the exterior of the vial210. In some instances, the sleeve 1680 can resemble the jacket 505described above. In various arrangements, the sleeve 1680 comprises heatshrink tubing, polyester, polyethylene, polypropylene, saran, latexrubber, polyisoprene, silicone rubber, or polyurethane.

With reference to FIGS. 31 and 32, in certain embodiments, the channelhousing member 1670 comprises a medical connector interface 1640, aradial extension 1672, and a sheath 1622. In some instances, the medicalconnector interface 1640, the radial extension 1672, and the sheath 1622are integrally formed of a unitary piece of material. In many instances,the channel housing member 1670 comprises a stiff material, such aspolycarbonate plastic.

The medical connector interface 1640 can resemble other medicalconnector interfaces described herein in many respects. In certainarrangements, the medical connector interface 1640 defines a proximalend of an extractor channel 1645. In some arrangements, the medicalconnector interface 1640 is offset from an axial center of the channelhousing member 1670.

In some arrangements, the medical connector interface 1640 isasymmetric, and in some instances, comprises an indentation 1641 at abase thereof. In certain instances, the indentation 1641 results fromone side of the medical connector interface 1640 having a more taperedand/or thinner sidewall than another side thereof, as illustrated inFIG. 32. In other instances, the indentation 1641 results from thesidewall being shaped differently on two or more sides of the medicalconnector interface 1640, while the thickness of the sidewall does notsubstantially vary at any given latitudinal cross-section of the medicalconnector interface 1640. As described below, in some instances, theindentation 1641 facilitates assembly of the adaptor 1600 and/or permitsthe use of a larger bag 1660.

In certain embodiments, the radial extension 1672 projects outward froman axial center of the channel housing member 1670. In somearrangements, the radial extension 1672 is located at the base of themedical connector interface 1640 such that the extractor channel 1645extends through the radial extension 1672. In further arrangements, theradial extension 1672 defines a bag insertion aperture 1674. In someinstances, a ledge 1676 (shown in FIGS. 30, 32, and 33) separates thebag insertion aperture 1674 from the base of the medical connectorinterface 1640. The bag insertion aperture 1674 can assume any of avariety of shapes. In the illustrated embodiment, the bag insertionaperture 1674 is substantially semicircular with the ledge 1676 defininga flat portion of the semicircle (see FIG. 30).

With reference to FIGS. 31 through 34, the sheath 1622 can resembleother sheaths disclosed herein in many respects. In some embodiments, anaxial length of the sheath 1622 is substantially perpendicular to theradial extension 1672. In some arrangements, the sheath 1622 defines atleast a distal portion of the extractor channel 1645. In some instances,the portion of the sidewall of the sheath 1622 defining a portion of theextractor channel 1645 is thinner than other portions of the sidewall(see FIGS. 32 and 33). In further arrangements, the sheath 1622 definesa cavity 1629 for housing at least a portion of the bag 1660. In someinstances, the extractor channel 1645 and the cavity 1629 are separatedby an inner wall 1627. The sheath 1622 can be generally hollow andterminate at a distal end 1623.

With reference to FIGS. 31, 32, and 34, in some embodiments, anextractor aperture 1646 extends through a sidewall of the sheath 1622 ata distal end of the extractor channel 1645. In some arrangements, theextractor aperture 1646 is substantially circular. In various instances,the diameter of the extractor aperture 1646 is between about 0.020inches and about 0.060 inches, between about 0.030 inches and about0.050 inches, or between about 0.035 inches and about 0.045 inches. Inother instances the diameter is greater than about 0.020 inches, greaterthan about 0.030 inches, or greater than about 0.035 inches. In stillother instances, the diameter is less than about 0.060 inches, less thanabout 0.050 inches, or less than about 0.045 inches. In some instances,the diameter is about 0.040 inches.

As described below, in certain arrangements, the extractor aperture 1646is configured to be adjacent the septum 216 when the adaptor 1600 iscoupled with the vial 210. In various instances, a center of theextractor aperture 1646 is spaced from a distal surface 1679 of theradial extension 1672 (see FIG. 32) by a distance of between about 0.25inches and about 0.35 inches, between about 0.28 inches and about 0.32inches, or between about 0.29 inches and about 0.31 inches. In otherinstances, the distance is greater than about 0.25 inches, greater thanabout 0.28 inches, or greater than about 0.29 inches. In still otherinstances, the distance is less than about 0.35 inches, less than about0.32 inches, or less than about 0.31 inches. In some instances, thedistance is about 0.305 inches.

With reference to FIGS. 31 and 34, in certain embodiments, a groove 1678extends distally from the extractor aperture 1646. In some arrangements,the groove 1678 extends along the length of the sheath 1622. In otherarrangements, the groove 1678 extends at an angle with respect to thelength of the sheath 1622. The groove 1678 can be substantiallystraight, or it can be curved. In some arrangements, the groove 1678 hasa substantially constant depth and width. In other arrangements, thedepth and/or width vary along a length of the groove 1678. In someinstances, the cross-sectional profile of the groove 1678 isasymmetrical, as shown in FIG. 34. Accordingly, the depth of the groove1678 can vary from one side of the groove 1678 to the other.

In various arrangements, the length of the groove 1678 is between about0.15 inches and about 0.35 inches, between about 0.20 inches and about0.30 inches, or between about 0.23 inches and about 0.27 inches. Inother arrangements, the length is greater than about 0.15 inches,greater than about 0.20 inches, or greater than about 0.23 inches. Instill other arrangements, the length is less than about 0.35 inches,less than about 0.30 inches, or less than about 0.27 inches. In someembodiments, the length is about 0.25 inches.

In various arrangements, the width of the groove 1678 is between about0.010 inches and about 0.030 inches, between about 0.015 inches andabout 0.025 inches, or between about 0.018 inches and about 0.022inches. In other arrangements, the width is greater than about 0.010inches, greater than about 0.015 inches, or greater than about 0.018inches. In still other arrangements, the width is less than about 0.030inches, less than about 0.025 inches, or less than about 0.022 inches.In some embodiments, the width is about 0.020 inches.

In various arrangements, the depth of the groove 1678, as measuredbetween the highest point and the lowest point of the cross-sectionalprofile of the groove 1678, is between about 0.020 inches and about0.040 inches, between about 0.025 inches and about 0.035 inches, orbetween about 0.030 inches and about 0.034 inches. In otherarrangements, the depth is greater than about 0.020 inches, greater thanabout 0.025 inches, or greater than about 0.030 inches. In still otherarrangements, the depth is less than about 0.040 inches, less than about0.035 inches, or less than about 0.034 inches. In some embodiments, thedepth is about 0.032 inches.

In some instances, it is desirable to remove substantially all of thefluid within the vial 210, such as when the fluid is a costlymedication. Accordingly, in certain arrangements, it is desirable forthe extractor aperture 1646 to be as close as possible to the septum 216when the adaptor 1600 is coupled with the vial 210 so that a maximumamount of fluid can be removed from the vial 210. However, the precisedimensions of the septum 216 or, more generally, of the cap 214 can varyamong different vials 210 of the same make and size. Further, theadaptor 1600 can be configured to couple with an assortment of vials 210that vary by size or by source of manufacture. These variations can alsoresult in variations in cap dimensions and, as a result, the location ofthe extractor aperture 1646 with respect to the septum 216.Advantageously, the groove 1678 can provide a fluid passageway to theextractor aperture 1646, even if the extractor aperture 1640 ispartially or completely obstructed by the septum 216. In many instances,the groove 1678 allows the removal of substantially all of the fluidcontents of the vial 210, regardless of the precise orientation of theextractor aperture 1646 with respect to the septum 216.

In some instances, the groove 1678 is sized and dimensioned such thatthe septum 216 does not obstruct the flow of fluid through the groove1678. In many arrangements, the septum 216 comprises a compliantmaterial that conforms to the shape of an item inserted therethrough,often forming a liquid-tight seal with the item. Accordingly, in someinstances, the edges of the groove 1678 are angled sufficiently sharplyand the depth of the groove 1678 is sufficiently large to prevent theseptum 216 from completely conforming to the shape of the groove 1678.Accordingly, a fluid passageway remains between the septum 216 and thevolume of the groove 1678 that is not filled in by the septum 216.

In some instances, the groove 1678 extends into the sheath 1622 at anangle, rather than directly toward the center of the sheath 1622. Insome instances, an angled configuration allows the groove 1678 to bedeeper than it could be otherwise. In some instances, the depth of thegroove 1678 is greater than the thickness of the sheath 1622.

With reference to FIGS. 30, 35, and 36, the plug 1601 is configured tosecure the bag 1660 to the channel housing member 1670. In somearrangements, the plug 1601 comprises a projection 1602 and a rim 1604.

In certain arrangements, the projection 1602 is configured to beinserted into an opening 1661 of the bag 1660 and to tension the bag1660 against the bag insertion aperture 1674 (see FIG. 30). In someinstances, the cross-sectional profile of the projection 1602 issubstantially complementary to that of the bag insertion aperture 1674.In the illustrated embodiment, the cross-sectional profile of theprojection 1602 is substantially semicircular. The projection 1602 cantaper toward a distal end thereof, allowing the projection to beinserted into the bag insertion aperture 1674 with relative ease. Inmany instances, contact between the projection 1602 and the bag 1660creates a substantially airtight seal, and contact between the bag 1660and the channel housing member 1670 creates a substantially airtightseal. In some instances, glue or some other adhesive is applied to theplug 1601, the bag 1660, and/or the channel housing member 1670 toensure a substantially airtight seal.

In some instances, the semicircular arrangement of the projection 1602and the bag insertion aperture 1674 facilitates assembly of the adaptor1600. The asymmetry of the arrangement can help to ensure that the plug1601 is oriented properly upon insertion thereof into the channelhousing member 1670. The asymmetry can also prevent the plug 1601 fromrotating within the channel housing member 1670. Other arrangements arealso possible for the interface between the plug 1601 and the channelhousing member 1670.

In certain arrangements, the rim 1604 extends along a portion of theperimeter of the plug 1601 and defines a recess 1605. In some instances,the recess 1605 is configured to accept a flange 1661 of the bag 1660(see FIG. 30), thereby allowing a distal surface of the rim 1604 tocontact a proximal surface of the radial extension 1672. In someinstances, an adhesive is applied to the distal surface of the rim 1604to help secure the plug 1601 to the channel housing member 1670.

In certain embodiments, the plug 1601 defines a regulator channel 1625.The regulator channel 1625 can extend from a regulator aperture 1650into the bag 1660 of an assembled adaptor 1600. In certain arrangements,the regulator aperture 1650 is exposed to the environment at theexterior of the assembled adaptor 1600. The regulator channel 1625 canpermit air to ingress to and/or egress from the bag 1660.

With reference to FIGS. 30 and 37 through 39, the cap connector 1630 canresemble the cap connectors described above in many ways. In variousinstances, the cap connector comprises one or more projections 1637and/or one or more slits 1639. In some arrangements, the cap connector1630 comprises a piercing member aperture 1632. In some instances, thepiercing member 1620 is inserted through the piercing member aperture1632 during assembly of the adaptor 1600.

In some instances, a proximal surface of the cap connector 1630 issubstantially planar. In further instances, a distal surface of theradial projection 1672 of the channel housing member 1670 is alsosubstantially planar. The two planar surfaces can abut one another in anassembled adaptor 1600. Advantageously, a large area of contact betweenthe cap connector 1630 and the radial projection 1672 can permit asecure attachment between these pieces via application of an adhesive,ultrasonic welding, or some other method.

With reference to FIG. 30, in some embodiments, the shroud 1690 isconfigured to couple with the cap connector 1630. The shroud 1690 canfrictionally engage the cap connector 1630, snap into the cap connector1630, or couple with the cap connector 1630 by any other suitable means.In some arrangements, the shroud 1690 comprises one or more indentations1694 that can provide traction for removing the shroud 1690 prior tousing the adaptor 1600. In other embodiments, the shroud 1690 comprisesa substantially smooth inner surface and a substantially smooth outersurface, and can resemble a right cylindrical tube. In some embodiments,the shroud is open at a proximal end 1692 and closed at a distal end1696. In other embodiments, the shroud 1690 is open at the proximal end1692 and open at the distal end 1696. In certain arrangements, theshroud 1690 is configured to enclose, substantially encircle, orotherwise shield the piercing member 1620 without contacting thepiercing member 1620. The shroud 1690 can prevent contamination ordamage of the piercing member 1620 that may result from accidentalcontact with the piercing member 1620 prior to use of the adaptor 1600.

FIG. 40 illustrates an embodiment of an adaptor 1700 in a disassembledstate. The adaptor 1700 can be coupled with a vial, such as the vial210. The adaptor 1700 resembles the adaptors described above in manyways, but differs in manners such as those discussed hereafter. Anysuitable combination of features, structures, or characteristicsdescribed with respect to the adaptor 1700 and/or any other adaptordescribed herein is possible.

In certain embodiments, the adaptor 1700 comprises a medical connector241, a housing member 1705, a bag 1760, a bag retainer 1770, a tip 1724,and/or a sleeve 1780. In some embodiments, the housing member 1705comprises a medical connector interface 1740, a cap connector 1730, anda sheath 1722, each of which can in many ways resemble the medicalconnector interfaces, cap connectors, and sheaths, respectively,described herein. The medical connector 241, the bag 1760, the tip 1724,and the sleeve 1780 can in many ways resemble the medical connectors,bags, tips, and the sleeve 1680, respectively, described herein. In someembodiments, a piercing member 1720 comprises the sheath 1722, the bagretainer 1770, and the tip 1724.

With reference to FIG. 41A, in certain embodiments, the cap connector1730 defines a regulator aperture 1750. In some embodiments, theregulator aperture 1750 is slightly offset from an axial center of thevial adaptor 1700. In some embodiments, the regulator aperture 1750 isin close proximity (e.g., adjacent) to an interface of the cap connector1730 and the medical connector interface 1740. Advantageously, theregulator aperture 1750 can be sufficiently small to prevent passagetherethrough of undesirable objects, and sufficiently large to vent theadaptor 1700 to atmosphere. A relatively small regulator aperture 1750can also permit the medical connector interface 1740 to be locatedrelatively centrally, thus helping to balance the adaptor 1700 andprevent accidental tipping when the adaptor 1700 is connected with avial.

With reference to FIG. 41B, in certain embodiments, the sheath 1722comprises a recessed surface 1723 at a distal end thereof. The recessedsurface 1723 can be substantially cylindrical, and can have a smallerouter diameter than an outer diameter of a more proximal portion of thesheath 1722. In some embodiments, the sheath 1722 defines a distal ledge1725. The distal ledge 1725 can extend between an outer surface 1726 ofthe sheath 1722 and the recessed surface 1723. In some embodiments, thesheath 1722 defines an extractor aperture 1746. In some embodiments, thesheath 1722 includes a groove 1778, such as the groove 1678, thatextends from the extractor aperture. In other embodiments, the sheath1722 does not include a groove 1778. The extractor aperture 1746 can belocated at a position distal of the base of the sheath 1722 such thatthe aperture 1746 is less likely to be covered by the septum 216 of thecap 214 when the adaptor 1700 is connected to a vial 200. In variousembodiments, the extractor aperture 1746 is positioned within a regioncovering about half, one-quarter, or one-eighth of the distance from thebase of the sheath 1722 to the end of the sheath 1722.

In some embodiments, the cap connector 1730 comprises a skirt 1736, suchas the skirt 736. The skirt 1736 can define one or more slits 1739,which can allow the cap connector 1730 to flex radially outward as theadaptor 1700 is being coupled with a vial. In some embodiments, aportion of a slit 1739 defines a notch 1738. The notch 1738 can resultfrom a molding process used to manufacture the housing member 1705. Insome embodiments, a removable tapered pin (not shown) is positioned suchthat the notch 1738 is formed around a proximal portion of the pin, andthe extractor aperture 1746 is formed around a distal portion of thepin. In further embodiments, the groove 1778 is also formed by aremovable piece which, in some embodiments, extends transversely fromthe tapered pin.

In some embodiments, the notch 1738 can assist in signaling to a userthe orientation of the extractor aperture 1746 when the adaptor 1700 iscoupled with a vial 200. For example, in some embodiments, a center ofthe extractor aperture 1746 and a center of the notch 1738 aresubstantially collinear along a straight line that is substantiallyperpendicular to a longitudinal axis of the sheath 1722. In certain ofsuch embodiments, if the extractor aperture 1746 is obscured by the vial200 and/or a portion of the cap connector 1730 (such as the skirt 1736)when the sheath 1722 is inside the vial 200, the radial orientation ofthe extractor aperture 1746 nevertheless can be determined byreferencing the radial orientation of the notch 1738, which is outsideof the vial 200. In some embodiments, a method of extracting fluid froma vial 200 includes directing the notch 1738 toward the ground to permitfluid to collect near the extractor aperture 1746.

With reference to FIG. 42, in some embodiments the bag 1760 comprises anelastic material and can be substantially bulbous when in an unexpandedstate. In certain embodiments, a distal portion 1761 of the bag 1760 isconvexly rounded, and can be substantially hemispherical. In furtherembodiments, the bag 1760 comprises a substantially cylindrical portion1762 that extends from the distal portion 1761. The bag 1760 can includea concavely rounded portion 1763 at a proximal end of the cylindricalportion 1762. In some embodiments, a radius of curvature of the distalportion 1761 of the bag 1760 is larger than a radius of curvature of theconcavely rounded portion 1763. In further embodiments, the diameter ofthe cylindrical portion 1762 and an axial distance between a tip 1764 ofthe distal end 1761 and a proximal end 1765 of the concavely roundedportion 1763 are substantially proportional to the maximum diameter andthe height, respectively, of a vial with which the adaptor 1700 isconfigured to be coupled.

In certain embodiments, the bag 1760 is configured to expand to fill asubstantial volume of a vial with which the adaptor 1700 is coupled. Invarious embodiments, the substantial volume filled by the bag 1760 is atleast about 40 percent, at least about 50 percent, at least about 60percent, at least about 70 percent, or at least about 80 percent of thevolume of the vial. In some embodiments, the bag 1760 is sized, shaped,and/or is sufficiently flexible to fill a substantial volume of a vialthat has a capacity of at least about 10 milliliters, at least about 20milliliters, or at least about 50 milliliters. In further embodiments,the bag 1760 is configured to fill a substantial volume of a vial thathas a capacity of at least about 100 milliliters or at least about 200milliliters. The bag 1760 can also be configured to fill other volumes.

In some embodiments, the bag 1760 comprises a lip 1766 or other regionof increased thickness extending outward from a proximal portion of thebag 1760. The lip 1766 can be disposed around a periphery of a proximalend 1767 of the bag 1760 and can aid in coupling the bag 1760 with thepiercing member 1720, such as in a manner described below. In someconfigurations, the increased thickness of the lip 1766 can increase theamount of force necessary to radially expand the lip 1766, thus causingthe lip 1766 to, in effect, grip more tightly a surface of an objectpositioned within it.

In some embodiments, the thickness of the bag 1760 varies from oneportion to another. For example, in some embodiments, the distal portion1761 of the bag 1760 is thinner and can be relatively stretchier or morecompliant than the proximal region. The variations in thicknesses of thebag 1760 can encourage the distal portion 1761 of the bag 1760 to expandmore than the proximal region, and can allow the proximal region to gripthe piercing member 1720 more effectively.

With reference to FIG. 43A, in certain embodiments, the bag retainer1770 defines a proximal portion 1771 and a distal portion 1772 havingdifferent thicknesses. Each of the respective thicknesses can besubstantially uniform. In certain embodiments, the proximal portion 1771has a thickness of no greater than about 20 thousandths of an inch, nogreater than about 15 thousandths of an inch, or no greater than about10 thousandths of an inch. In some embodiments, the thickness is about10 thousandths of an inch. Other thicknesses are possible.

In some embodiments, each of the proximal and distal portions 1771, 1772is substantially cylindrical. In further embodiments, an outer surface1773 of the bag retainer 1770 is also substantially cylindrical. In someembodiments, the proximal portion 1771 is thinner than the distalportion 1772 such that the distal portion 1772 defines an inner shelf1774. The inner shelf 1774 can aid in securing the bag 1760 to thepiercing member 1720.

With reference to FIG. 43B, in some embodiments, the bag retainer 1770comprises an outer surface 1773 that is curved along a longitudinallength thereof such that the thickness of the proximal and distalportions 1771, 1772 varies along the longitudinal length. In someembodiments, the bag retainer 1770 is thicker towards the longitudinalcenter thereof, which can provide the bag retainer 1770 with addedstrength. In many embodiments, the outer surface 1773 is substantiallysmooth, which can allow the bag retainer 1770 to pass through the septumof a vial relatively easily. The bag retainer 1770 can comprise avariety of materials, and in some embodiments, comprises polycarbonateplastic.

FIG. 44A illustrates an embodiment of the vial adaptor 1700 in anassembled state. As shown, in certain embodiments, the sleeve 1780 canretain the tip 1724 and the bag retainer 1770 in close proximity (e.g.,adjacent) to each other. In some embodiments, the sleeve 1780 comprisesan elastic material, which can be stretched radially outward about thetip 1724 and the bag retainer 1770. In many embodiments, the sleeve 1780is forced toward the proximal end of the sheath 1722 and away from thetip 1724 and the bag retainer 1770 as the piercing member 1720 isadvanced through the septum of a vial, which can permit the tip 1724 toseparate from the bag retainer 1770 when the adaptor 1700 is coupledwith the vial.

With reference to FIG. 44B, in certain embodiments, a portion of the bag1760 is retained between the sheath 1722 and the bag retainer 1770. Insome embodiments, the lip 1766 of the bag 1760 is held between thedistal ledge 1725 of the sheath 1722 and the inner shelf 1774 of the bagretainer 1770. The distal ledge 1725 and the inner shelf 1774 cansubstantially prevent longitudinal movement of the bag 1760 relative tothe sheath 1722. In further embodiments, a portion of the bag 1760 isretained between the distal portion 1772 of the bag retainer 1770 andthe recessed surface 1723 of the sheath 1722.

In some embodiments, the sheath 1722 and the bag retainer 1770 retainthe bag 1760 in substantially airtight engagement such that air enteringthe sheath from without a vial can expand the bag yet be preventedsubstantially from flowing into the contents of the vial. In someembodiments, the bag retainer 1770 is solvent-bonded to the sheath 1722via ethylene dichloride or any other suitable manner.

In certain embodiments, a surface of the bag 1760, such as an interiorsurface 1768 of the bag 1760, is lubricated. The lubrication canfacilitate placement of the bag 1760 within the sheath 1722, such asduring assembly of the adaptor 1700, and/or can facilitate deployment ofthe bag 1760, such as when fluid is removed from a vial with which theadaptor 1700 is coupled. In certain embodiments, lubricant applied tothe interior surface 1768 of the bag can reduce friction at an interfacebetween the bag 1760 and the sheath 1722. In some embodiments, thelubricant can reduce friction at one or more interfaces between separateportions of the bag 1760, such as when the bag 1760 is doubled backwithin the sheath 1722. The bag 1760 can be lubricated in any suitablemanner, such as those described above with respect to the bag 260. Incertain embodiments, the bag 1760 is lubricated with fluoro siliconeoil.

In some embodiments, the interior surface 1768 of the bag 1760 istextured. For example, the interior surface 1768 can be grooved orroughened, or it can include bumps, ridges, lines, or protrusions orindentations arranged, for example, in a regular array, in an irregularpattern, or substantially randomly. The texturing can resemble thefinish of an article that has been exposed to bead blasting or sandblasting, e.g., a randomly spaced grouping of bumps and divots. In someembodiments, the textured surface 1768 reduces the surface area of thebag 1760 that is in contact with other portions of the bag 1760, such aswhen the bag 1760 is doubled back, folded, pleated, bunched, orotherwise positioned within the sheath 1722. Reducing the total surfacearea of the bag 1760 that contacts itself can improve the agingproperties of the bag 1760, and can extend the shelf life of anassembled adaptor 1700. For example, some materials from which the bag1760 can be manufactured tend to stick or bond to themselves over time,which can inhibit ready deployment of the bag 1760.

In some embodiments, a textured interior surface 1768 can inhibitlubricant from beading on the surface 1768. The textured surface 1768thus can promote a relatively uniform distribution of the lubricant,thereby encouraging ready deployment of the bag 1760. In someembodiments, an exterior surface of the bag 1760 is textured, either inaddition to or instead of texturing of the interior surface 1768.

In certain embodiments, the tip 1724 comprises a stem, stalk, orproximal extension 1790 such as the proximal extension 224 a describedabove. In some embodiments, the proximal extension 1790 tapers toprogressively smaller transverse cross-sectional areas toward itsproximal end. In some embodiments, the proximal extension 1790 comprisesa substantially cylindrical portion 1792. The proximal extension 1790can transition from the substantially cylindrical portion 1792 to asubstantially frustoconical portion 1794, and in further embodiments,can transition to a substantially curved or rounded end 1796. Otherarrangements are also possible. For example, in some embodiments, theproximal extension 1790 is substantially conical or substantiallytubular, and in some embodiments, the proximal extension 1790 includesone or more of the substantially cylindrical portion 1792, thesubstantially frustoconical portion 1794, and the substantially roundedend 1796.

In certain embodiments, the proximal extension 1790 is configured toexert relatively little, if any, pressure on the bag 1760 within thesheath 1722, and can be relatively unlikely to puncture or tear the bag1760. For example, in some embodiments, as the adaptor 1700 is advancedinto a vial 200, the tip 1724 might tilt or rotate such that alongitudinal axis thereof is skewed relative to a longitudinal axis ofthe sheath 1722, which can cause the proximal extension 1790 to pressthe bag 1760 against the inner wall of the sheath 1722. In someembodiments, the proximal extension 1790 is sized and shaped such that arelatively large area thereof (as compared, e.g., with an edge or apoint) contacts the bag 1760 when the tip 1724 is not axially alignedwith the sheath 1722. For example, in some embodiments, thefrustoconical portion 1794 provides a relatively large area forcontacting the bag 1760 regardless of the direction in which theproximal extension 1790 is tilted or rotated relative to the sheath1722.

With reference again to FIG. 40, in certain embodiments, a method ofassembling the adaptor 1700 includes providing a housing member 1705having a sheath 1722. In some embodiments, the method includes attachinga bag 1760 to the sheath 1722, and in further embodiments, to the distalend of the sheath 1722. The method can include inverting the bag 1760and/or advancing a portion of the bag 1760 into the sheath 1722. In someembodiments, the method includes advancing a bag retainer 1770 over aportion of the bag 1760, which can thereby secure the bag 1760 to thesheath 1722. In some embodiments, the method includes advancing aportion of a tip 1724 inside the bag retainer 1770. The method caninclude placing or sliding a sleeve 1780 over at least a portion of thetip 1724 and at least a portion of the bag retainer 1770.

In some embodiments, a method for assembling the adaptor 1700 includeslubricating the bag 1760. For example, the method can includeintroducing or applying an amount of one or more of the lubricantslisted above to an interior region of the bag 1760. In some embodiments,the lubricant is applied before the bag 1760 is secured to the sheath1722. In other embodiments, the bag is secured to the sheath 1722 beforethe lubricant is introduced into the bag. For example, in someembodiments, lubricant can be inserted through the regulator aperture1750 (see FIG. 41A) into the bag 1760.

In some instances, introducing lubricant after the bag 1760 is attachedto the sheath 1722 can facilitate securing the bag 1760 to the sheath1722. For example, in some embodiments, it can be difficult toselectively apply lubricant to the bag 1760 in a manner that avoidslubricating undesirable portions of the bag 1760, such as the proximalend thereof. In certain of such embodiments, lubricating the proximalend of the bag 1760 can cause the bag 1760 to slip relative to thesheath 1722, such as when the bag retainer 1770 is applied, and caninhibit or prevent creation of a seal between the bag 1760 and thesheath 1722. In some embodiments, by securing the bag 1760 to the sheath1722 prior to introducing lubricant to the bag 1760, a substantiallyfluid-tight seal can be formed between the bag 1760 and the sheath 1722.In further embodiments, the seal thus formed can prevent the lubricantfrom advancing between the bag 1760 and the sheath 1722, and can therebymaintain a tight seal that can substantially prevent air from leakinginto the vial 200, and substantially prevent fluid from leaking out ofthe vial 200, between the bag 1760 and the sheath 1722.

FIG. 45 illustrates an embodiment of a housing member 1805, such as thehousing member 1705, which can be compatible with the adaptor 1700. Insome embodiments, the housing member 1805 comprises a medical connectorinterface 1840, a cap connector 1830, and a sheath 1822.

In certain embodiments, the housing member 1805 defines a relativelylarge regulator aperture 1850. In some embodiments, at least a portionof the regulator aperture 1850 is defined by the medical connectorinterface 1840, which can include a recess 1880. The recess 1880 cancomprise a groove or indentation that extends from a location distal ofa proximal end 1882 of the interface 1840 to a distal end 1884 of theinterface 1840. The recess 1880 can increase in width and depth towardthe regulator aperture 1850.

In some embodiments, the regulator aperture 1850 and/or the recess 1880facilitate assembly of the adaptor 1700. For example, in someembodiments, a bag 1760 is secured to the sheath 1822. Lubricant canthen be introduced to the bag 1760 via the regulator aperture 1850. Insome embodiments, the size of the regulator aperture 1850 issufficiently large to receive an instrument 1886, such as a needle or ahollow tube, configured to introduce lubricant into the bag 1760. Infurther embodiments, the recess 1880 is sized and shaped to guide a tipof the instrument 1886 toward and, in still further embodiments, intothe regulator aperture 1850. For example, in the illustrated embodiment,the recess 1880 is substantially shaped as a partial paraboloid thatincreases in size toward the regulator aperture 1850. A tip of theinstrument 1886 contacting a proximal end of the recess 1880 thus can besmoothly directed distally and radially inward along a length of themedical connector interface 1840 toward the aperture 1850.

With continued reference to FIG. 45, in some embodiments, the proximalend 1882 of the medical connector interface 1840 is configured toreceive a medical connector 241 (see, e.g., FIG. 40). In someembodiments, solvent is applied to one or more surfaces of the proximalend 1882 of the interface 1840 and/or one or more surfaces of themedical connector 241, and the medical connector 241 is pressed onto theinterface 1840. In some embodiments, one or more of the interface 1840and the portion of the medical connector 241 that is configured toreceive the interface 1840 comprises plastic, such as polycarbonateplastic, that substantially liquefies upon application of the solvent.

In the illustrated embodiment, the interior and exterior surfaces of theproximal end 1882 of the medical connector interface 1840 aresubstantially smooth. In some instances, a relatively smooth proximalend 1882 can permit ready movement of the medical connector 241 relativeto the interface 1840 as these components are being joined, which canreduce stresses in an assembled adaptor 1700. For example, in someembodiments, the medical connector 241 is placed on the medicalconnector interface 1840 after solvent has been applied to and hassubstantially liquefied a portion of the connector 241 and/or theproximal end 1882 of the interface 1840. As the connector 241 is forceddistally onto the interface 1840, fluid pressure can arise that urgesthe connector 241 in a proximal direction. The connector 241 can thusnaturally settle to a position that reduces or eliminates stresses atthe junction of the connector 241 and the connector interface 1840 asthe assembled components cure.

FIG. 46 illustrates another embodiment of the housing member 1805. Inthe illustrated embodiment, the proximal end 1882 of the medicalconnector interface 1840 includes one or more engagement members suchas, for example, threads 1890. The threads 1890 can interface withcomplementary threading on the medical connector 241 to encourage atight seal between the connector 241 and the connector interface 1840.In some embodiments, solvent is applied to one or more of the connector241 and the connector interface 1840.

FIG. 47 illustrates an embodiment of a housing member 1905, such as thehousing members 1705, 1805, which can be compatible with the adaptor1700. In some embodiments, the housing member 1905 includes a sheath1922 that defines a receiving space, such as a receptacle or cavity1910. The sheath 1922 can include an outer wall 1930 and an inner rim1932 that at least partially define the cavity 1910. In someembodiments, the outer wall 1930 and the inner rim 1932 are shapedsubstantially as concentric hollow cylinders. The cavity 1910 can be ata distal end of the sheath 1922, and in some embodiments, issubstantially within the sheath 1922. The cavity 1910 can be adapted toreceive at least a portion of the bag 1760, such as a proximal end 1767thereof.

FIG. 48 illustrates an embodiment of the bag 1760 configured to couplewith the sheath 1922. The proximal end 1767 of the bag 1760 can be sizedand shaped to be received within the cavity 1910. In some embodiments,an inner dimension (e.g., inner diameter) of the proximal end 1767 isslightly larger than an outer dimension (e.g., outer diameter) of theinner rim 1932, and the proximal end 1767 can be urged into the cavity1910 without radially stretching the bag 1760. In other embodiments, theinner dimension of the proximal end 1767 is about the same or slightlyless than the outer dimension of the inner rim 1932 and the proximal end1767 is stretched radially outward in order to be placed over the innerrim 1932. An outer dimension of the proximal end 1767 can be slightlysmaller than an inner dimension of the outer wall 1930 of the sheath1922.

In some embodiments, the proximal end 1767 of the bag 1760 defines asubstantially uniform thickness. In some embodiments, the bag 1760 ismanufactured via dip molding that produces a lip 1766 (see FIG. 42) atthe proximal end 1767 of the bag 1760. Because the thickness of the lip1766 can be difficult to control in some dip molding processes, the lip1766 can be removed such that the thickness of the proximal end 1767 ismore predictable or more controllable, which can facilitate insertion ofthe proximal end 1767 into the cavity 1910. In other embodiments, thebag 1760 can include the lip 1766.

The proximal end 1767 of the bag 1760 can be adhered to the sheath 1922to form a substantially fluid-tight seal therewith. In some embodiments,a quantity of adhesive, such as glue, is introduced into the cavity1910. The adhesive can comprise a low viscosity fluid capable of flowingabout the perimeter of the inner rim 1932, and can be capable of wickingin a distal direction along the outer surface of the inner rim 1932 andthe inner surface of the outer wall 1930. A sufficient amount ofadhesive can be applied to substantially cover a base portion of thecavity 1910. Any suitable adhesive may be used, including cyanoacrylate.

In some embodiments, the adhesive is configured to create a very rapidor virtually instantaneous bond between the bag 1760 and the sheath 1922such that the bag 1760 cannot be repositioned once it has been adheredto the sheath 1922. For example, in some embodiments, when the bag 1760comprises polyisoprene, the sheath 1922 comprises polycarbonate plastic,and the adhesive comprises cyanoacrylate, the bag 1760 can be adhered tothe sheath 1922 upon contacting the adhesive.

In some embodiments, the cavity 1910 is sufficiently deep and/or theamount of adhesive used is sufficiently small that insertion of the bag1760 into the cavity 1910 does not force any adhesive from the cavity1910. Accordingly, a distal portion 1761 of the bag 1760 can be insertedinto the sheath 1922 without being adhered to the sheath 1922, which canallow for ready deployment of the bag 1760.

In some embodiments, the bag 1760 can be attached to the sheath 1922without a bag retainer 1770 (see FIG. 40), which can reduce the materialcosts of and/or the number of manufacturing steps for producing anadaptor 1700. In other embodiments, a bag retainer 1770 can be used withthe sheath 1922. For example, the bag retainer 1770 can be sized andshaped to fit within the cavity 1910 in close engagement with theproximal end 1767 of the bag 1760. In other embodiments, the bagretainer 1770 can be positioned within the bag 1760 and can provide anoutwardly projecting force to create and/or maintain a substantiallyfluid-tight seal between the bag 1760 and the inner surface of the outerwall 1930.

With reference again to FIG. 47, in some embodiments, the sheath 1922comprises a proximal section 1940 and a distal section 1942, asindicated by a dashed line in the illustrated example. The distalsection 1942 can be manufactured separately from the proximal section1940 and can be attached to a bag 1760 to form a sub-assembly. Thesub-assembly may be independently tested to determine whether asubstantially fluid-tight seal has been formed between the bag 1760 andthe distal section 1942. An acceptable sub-assembly then can be attachedto the proximal section 1940 of the sheath 1922 in any suitable manner,such as by ultrasonic welding. Providing a two-part sheath 1922 in thismanner can reduce the material costs of producing an adaptor 1700 bypermitting disposal of only a small portion of the sheath 1922, ratherthan disposal of a full housing member 1905, should attachment of a bag1760 to the sheath 1922 fail to create a desired seal.

FIG. 49 illustrates an embodiment of a housing member 2005, such as thehousing members 1705, 1805, 1905, which can be compatible with theadaptor 1700. The housing member 2005 includes a cap connector 2030 anda sheath 2022 that defines an extractor aperture 2046. In someembodiments, housing member 2005 is configured for use with relativelylarge vial 200. For example, the sheath 2022 can be relatively long, asdiscussed further below, and the cap connector 2030 can define arelatively large inner dimension (e.g., inner diameter) to accommodate arelatively large cap 214.

In some embodiments, it is desirable to space the bag 1760 sufficientlyfar from the underside of the cap 214, or sufficiently far from theextractor aperture 2046, to prevent fluid from becoming inaccessible tothe extractor aperture 2046 as the bag 1760 expands. For example, insome embodiments, as fluid is removed from a vial 200, the bag 1760 canexpand to contact a sidewall of the vial 200, and can form asubstantially fluid-tight seal therewith. If the fluid-tight seal iscreated before a portion of liquid in the vial 200 has moved to a regionproximal of the bag 1760, this portion of liquid can effectively betrapped in a distal region of the vial 200, thus becoming inaccessibleto the extractor aperture 2046.

On the other hand, in some embodiments, it can be desirable to locatethe proximal end 1767 of the bag 1760 sufficiently close to theunderside of the cap 214, or sufficiently close to the extractoraperture 2046, that the sidewalls of the vial 200 do not significantlyinhibit expansion of the bag 1760. For example, if the bag 1760 hasexpanded to contact the bottom and side walls of the vial 200 before allof the fluid in the vial 200 has been removed, it can be difficult forsome embodiments of the bag 1760 to expand in a proximal direction asadditional fluid is removed from the vial 200.

The foregoing factors can be considered or balanced in developingvarious embodiments of the adaptor 1700. In some embodiments, the sheath2022 is configured to position the proximal end 1767 of the bag 1760 atabout the longitudinal center of a vial 200 with which the adaptor 1700is to be used. In other embodiments, the sheath 2022 is configured tospace the proximal end 1767 of the bag 1760 from the underside of thecap 214 of the vial 200 by no less than about ¼, no less than about ⅓,or no less than about ½ the longitudinal distance between the undersideof a cap 214 and a bottom wall of the vial 200. In various embodiments,a distance between the extractor aperture 2046 and a distal end of thesheath 2022 is greater than a minimum outer dimension (e.g., minimumouter diameter) of the proximal end of the sheath 2022 by a factor of noless than about: 1 4, 8, or 10.

Discussion of the various embodiments disclosed herein has generallyfollowed the embodiments illustrated in the figures. However, theparticular features, structures, or characteristics of any embodimentsdiscussed herein may be combined in any suitable manner, as would beapparent to one of ordinary skill in the art from this disclosure, inone or more separate embodiments not expressly illustrated or described.

Similarly, it should be appreciated that in the above description ofembodiments, various features are sometimes grouped together in a singleembodiment, figure, or description thereof for the purpose ofstreamlining the disclosure and aiding in the understanding of one ormore of the various inventive aspects. This method of disclosure,however, is not to be interpreted as reflecting an intention that anyclaim require more features than are expressly recited in that claim.Moreover, any components, features, or steps illustrated and/ordescribed in a particular embodiment herein can be applied to or usedwith any other embodiment(s). Thus, it is intended that the scope of theinventions herein disclosed should not be limited by the particularembodiments described above, but should be determined only by a fairreading of the claims that follow.

1. (canceled)
 2. A vial adaptor capable of removing medicinal fluid froma vial, the adaptor comprising: a cap connector capable of coupling theadaptor to the vial; a piercing member having an outer surface extendingfrom a base of the cap connector, wherein the piercing member is capableof being inserted into the vial when the adaptor is coupled to the vial;a sleeve surrounding at least a portion of the piercing member, whereinat least a portion of the sleeve is forced toward a proximal end of thepiercing member when the piercing member is inserted into the vial, andwherein the sleeve remains exterior to the vial when the adaptor iscoupled to the vial; and an extractor aperture disposed along a sidewallof the outer surface, wherein at least a portion of the extractoraperture has an elongate dimension, and wherein the extractor apertureprovides a fluid passageway to an extractor channel, even if theextractor aperture is partially obstructed by a septum of the vial whenthe adaptor is coupled to the vial.
 3. The vial adaptor of claim 2,wherein the sleeve is positioned distal to the extractor aperture whenthe adaptor is not coupled to the vial.
 4. The vial adaptor of claim 2,wherein the sleeve comprises an elastic material.
 5. The vial adaptor ofclaim 2, wherein the sleeve is positioned proximally of at least adistal end of the extractor aperture when the adaptor is coupled to thevial.
 6. The vial adaptor of claim 2, wherein the extractor apertureextends along at least about one-eighth of a length of the piercingmember.
 7. The vial adaptor of claim 2, wherein the extractor apertureis positioned adjacent the septum when the adaptor is coupled to thevial, and wherein the adaptor is capable of removing medicinal fluidfrom the vial while leaving no more than a small amount of medicinalfluid in the vial.
 8. The vial adaptor of claim 2, wherein at least adistal end of the sleeve is forced toward the proximal end of thepiercing member when the piercing member is inserted into the vial. 9.The vial adaptor of claim 2, wherein the entire sleeve is forced towardthe proximal end of the piercing member when the piercing member isinserted into the vial.
 10. The vial adaptor of claim 2, wherein acenter of the extractor aperture is spaced from the base by a distanceof less than about 0.35 inches.
 11. A method of withdrawing medicinalfluid from a vial, the method comprising: providing a vial adaptor forcoupling to the vial, the adaptor comprising: a cap connector capable ofcoupling the adaptor to the vial; a piercing member having a sidewallextending from a base of the cap connector, the piercing member capableof being inserted into the vial when the adaptor is coupled to the vial;a sleeve surrounding at least a portion of the piercing member; and anextractor aperture disposed along the sidewall of the piercing member,wherein at least a portion of the extractor aperture has an elongatedimension, and wherein the extractor aperture provides a fluidpassageway to an extractor channel, even if the extractor aperture ispartially obstructed by a septum of the vial when the adaptor is coupledto the vial; coupling the adaptor to the vial, wherein the extractoraperture is in fluid communication with an interior of the vial when theadaptor is coupled to the vial, wherein coupling the adaptor to the vialforces at least a portion of the sleeve toward a proximal end of thesidewall, and wherein the sleeve remains exterior to the vial when theadaptor is coupled to the vial; and withdrawing medicinal fluid from thevial.
 12. The method of claim 11, wherein prior to coupling the adaptorto the vial, the sleeve is positioned distal of the extractor aperture.13. The method of claim 11, wherein the sleeve comprises an elasticmaterial.
 14. The method of claim 11, wherein coupling the adaptor tothe vial further comprises moving the sleeve proximally of at least adistal end of the extractor aperture.
 15. The method of claim 11,wherein the extractor aperture extends along at least about one-eighthof a length of the piercing member.
 16. The method of claim 11, whereincoupling the adaptor to the vial comprises positioning the extractoraperture adjacent to the septum, and wherein the adaptor is capable ofremoving medicinal fluid from the vial while leaving no more than asmall amount of medicinal fluid in the vial.
 17. The method of claim 11,wherein forcing at least a portion of the sleeve toward the proximal endof the sidewall comprises forcing a distal end of the sleeve toward theproximal end of the sidewall.
 18. The method of claim 11, whereinforcing at least a portion of the sleeve toward the proximal end of thesidewall comprises forcing the entire sleeve toward the proximal end ofthe sidewall.
 19. The method of claim 11, wherein a center of theextractor aperture is spaced from the base by a distance of less thanabout 0.35 inches.
 20. A method of manufacturing a vial adaptor capableof removing medicinal fluid from a vial, the method comprising: formingthe adaptor comprising: a cap connector capable of coupling the adaptorto the vial; a piercing member having a sidewall extending from a baseof the cap connector, the piercing member capable of being inserted intothe vial when the adaptor is coupled to the vial; and an extractoraperture along the sidewall of the piercing member, wherein at least aportion of the extractor aperture has an elongate dimension, and whereinthe extractor aperture provides a fluid passageway to an extractorchannel, even if the extractor aperture is partially obstructed by aseptum of the vial when the adaptor is coupled to the vial; andpositioning a sleeve around at least a portion of the piercing member,wherein at least a portion of the sleeve is forced toward a proximal endof the sidewall when the piercing member is inserted into the vial, andwherein the sleeve remains exterior to the vial when the adaptor iscoupled to the vial.
 21. The method of claim 20, wherein positioning thesleeve comprises positioning the sleeve distal of the extractor aperturewhen the adaptor is not coupled to the vial.
 22. The method of claim 20,further comprising forming the sleeve from an elastic material.
 23. Themethod of claim 20, wherein forming the adaptor comprises forming theaperture along at least about one-eighth of a length of the piercingmember.
 24. The method of claim 20, wherein forming the adaptorcomprises forming the extractor aperture on the sidewall of the piercingmember in a position where the extractor aperture is located adjacentthe septum when the adaptor is coupled with the vial.
 25. The method ofclaim 20, wherein positioning the sleeve around at least a portion ofthe piercing member further comprises positioning the sleeve in alocation where a distal end of the sleeve is forced toward the proximalend of the sidewall when the piercing member is inserted into the vial.26. The method of claim 20, wherein positioning the sleeve around atleast a portion of the piercing member further comprises positioning thesleeve in a location where the entire sleeve is forced toward theproximal end of the sidewall when the piercing member is inserted intothe vial.
 27. The method of claim 20, wherein a center of the extractoraperture is spaced from the base by a distance of less than about 0.35inches.